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Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance.

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Title: Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance.
Authors: Marsh AP; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia., Heron D; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; Groupe de Recherche Clinique (GRC) `Déficience Intellectuelle et Autisme' UPMC, Paris, France.; Centre de Référence `Déficiences Intellectuelles de Causes Rares', Paris, France., Edwards TJ; Queensland Brain Institute, University of Queensland, St. Lucia, Brisbane, Australia.; School of Medicine, University of Queensland, Herston, Brisbane, Australia., Quartier A; IGBMC, Université de Strasbourg, CNRS, INSERM, UMR7104 U964, Strasbourg, France., Galea C; Drug Delivery, Disposition and Dynamics (D4), Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria, Australia., Nava C; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France., Rastetter A; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France., Moutard ML; AP-HP, Hôpital Trousseau, Service de Neuropédiatrie, Paris, France.; UPMC, GRC ConCer-LD, Sorbonne Université, Paris, France.; Centre de Référence `Neurogénétique', Paris, France., Anderson V; Developmental Imaging and Child Neuropsychology Research Groups, Murdoch Childrens Research Institute, Parkville, Victoria, Australia., Bitoun P; Génétique Médicale, CHU Paris Nord, Hôpital Jean Verdier, Bondy, France., Bunt J; Queensland Brain Institute, University of Queensland, St. Lucia, Brisbane, Australia., Faudet A; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France., Garel C; AP-HP GHUEP, Hôpital Armand Trousseau, Service de Radiologie, Paris, France., Gillies G; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia., Gobius I; Queensland Brain Institute, University of Queensland, St. Lucia, Brisbane, Australia., Guegan J; iCONICS Facility, ICM, Paris, France., Heide S; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; Groupe de Recherche Clinique (GRC) `Déficience Intellectuelle et Autisme' UPMC, Paris, France., Keren B; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France., Lesne F; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France., Lukic V; Bioinformatics Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia., Mandelstam SA; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.; Florey Institute of Neuroscience and Mental Health, Melbourne, Victoria, Australia.; Department of Radiology, University of Melbourne, Royal Children's Hospital, Parkville, Victoria, Australia., McGillivray G; Victorian Clinical Genetics Services, Murdoch Childrens Research Institute, Parkville, Victoria, Australia., McIlroy A; Developmental Imaging and Child Neuropsychology Research Groups, Murdoch Childrens Research Institute, Parkville, Victoria, Australia., Méneret A; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Neurologie, Paris, France., Mignot C; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; Groupe de Recherche Clinique (GRC) `Déficience Intellectuelle et Autisme' UPMC, Paris, France.; Centre de Référence `Déficiences Intellectuelles de Causes Rares', Paris, France., Morcom LR; Queensland Brain Institute, University of Queensland, St. Lucia, Brisbane, Australia., Odent S; Service de Génétique Clinique, Centre de Référence CLAD-Ouest, CHU Rennes, Rennes, France.; UMR 6290 CNRS, IGDR Institut de Génétique et Développement de Rennes, Université de Rennes 1, Rennes, France., Paolino A; Queensland Brain Institute, University of Queensland, St. Lucia, Brisbane, Australia., Pope K; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia., Riant F; AP-HP, Groupe Hospitalier Saint-Louis -La Riboisière -Fernand Vidal, Laboratoire de Génétique, Paris, France., Robinson GA; Neuropsychology Research Unit, School of Psychology, University of Queensland, Brisbane, Australia., Spencer-Smith M; Developmental Imaging and Child Neuropsychology Research Groups, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; School of Psychological Sciences and Monash Institute of Cognitive and Clinical Neurosciences, Monash University, Clayton, Victoria, Australia., Srour M; Department of Pediatrics, Montreal Children's Hospital, McGill University, Montreal, Quebec, Canada.; Department of Neurology and Neurosurgery, McGill University Health Center, Montreal, Quebec, Canada., Stephenson SE; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia., Tankard R; Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.; Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia., Trouillard O; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France., Welniarz Q; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.; Institut de Biologie Paris Seine, Neuroscience Paris Seine, Sorbonne Universités, UPMC Univ Paris 06, INSERM, CNRS, Paris, France., Wood A; Developmental Imaging and Child Neuropsychology Research Groups, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; School of Life and Health Sciences, Aston University, Birmingham, UK., Brice A; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France., Rouleau G; Department of Neurology and Neurosurgery, McGill University Health Center, Montreal, Quebec, Canada.; Montreal Neurological Institute and Hospital, McGill University, Montréal, Quebec, Canada., Attié-Bitach T; INSERM U1163, Laboratory of Embryology and Genetics of Congenital Malformations, Paris-Descartes University, Sorbonne Paris Cité and Imagine Institute, Paris, France.; AP-HP, Hôpital Necker-Enfants Malades, Département de Génétique, Paris, France., Delatycki MB; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.; Victorian Clinical Genetics Services, Parkville, Victoria, Australia., Mandel JL; IGBMC, Université de Strasbourg, CNRS, INSERM, UMR7104 U964, Strasbourg, France.; Laboratoires de Génétique, Institut de Génétique Médicale d'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France., Amor DJ; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia., Roze E; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Neurologie, Paris, France., Piton A; IGBMC, Université de Strasbourg, CNRS, INSERM, UMR7104 U964, Strasbourg, France.; Laboratoires de Génétique, Institut de Génétique Médicale d'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France., Bahlo M; Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.; Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia., Billette de Villemeur T; Centre de Référence `Déficiences Intellectuelles de Causes Rares', Paris, France.; AP-HP, Hôpital Trousseau, Service de Neuropédiatrie, Paris, France.; UPMC, GRC ConCer-LD, Sorbonne Université, Paris, France.; INSERM U1141, Paris, France., Sherr EH; Department of Neurology, UCSF Benioff Children's Hospital, San Francisco, California, USA., Leventer RJ; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.; Neuroscience Research Group, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; Department of Neurology, University of Melbourne, Royal Children's Hospital, Parkville, Victoria, Australia., Richards LJ; Queensland Brain Institute, University of Queensland, St. Lucia, Brisbane, Australia.; University of Queensland, School of Biomedical Sciences, St. Lucia, Brisbane, Australia., Lockhart PJ; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia., Depienne C; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; IGBMC, Université de Strasbourg, CNRS, INSERM, UMR7104 U964, Strasbourg, France.; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.; Laboratoires de Génétique, Institut de Génétique Médicale d'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Source: Nature genetics [Nat Genet] 2017 Apr; Vol. 49 (4), pp. 511-514. Date of Electronic Publication: 2017 Feb 27.
Publication Type: Journal Article
Journal Info: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE
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  Data: Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance.
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  Data: <searchLink fieldCode="AU" term="%22Marsh+AP%22">Marsh AP</searchLink>; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Heron+D%22">Heron D</searchLink>; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; Groupe de Recherche Clinique (GRC) `Déficience Intellectuelle et Autisme' UPMC, Paris, France.; Centre de Référence `Déficiences Intellectuelles de Causes Rares', Paris, France.<br /><searchLink fieldCode="AU" term="%22Edwards+TJ%22">Edwards TJ</searchLink>; Queensland Brain Institute, University of Queensland, St. Lucia, Brisbane, Australia.; School of Medicine, University of Queensland, Herston, Brisbane, Australia.<br /><searchLink fieldCode="AU" term="%22Quartier+A%22">Quartier A</searchLink>; IGBMC, Université de Strasbourg, CNRS, INSERM, UMR7104 U964, Strasbourg, France.<br /><searchLink fieldCode="AU" term="%22Galea+C%22">Galea C</searchLink>; Drug Delivery, Disposition and Dynamics (D4), Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Nava+C%22">Nava C</searchLink>; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.<br /><searchLink fieldCode="AU" term="%22Rastetter+A%22">Rastetter A</searchLink>; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.<br /><searchLink fieldCode="AU" term="%22Moutard+ML%22">Moutard ML</searchLink>; AP-HP, Hôpital Trousseau, Service de Neuropédiatrie, Paris, France.; UPMC, GRC ConCer-LD, Sorbonne Université, Paris, France.; Centre de Référence `Neurogénétique', Paris, France.<br /><searchLink fieldCode="AU" term="%22Anderson+V%22">Anderson V</searchLink>; Developmental Imaging and Child Neuropsychology Research Groups, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Bitoun+P%22">Bitoun P</searchLink>; Génétique Médicale, CHU Paris Nord, Hôpital Jean Verdier, Bondy, France.<br /><searchLink fieldCode="AU" term="%22Bunt+J%22">Bunt J</searchLink>; Queensland Brain Institute, University of Queensland, St. Lucia, Brisbane, Australia.<br /><searchLink fieldCode="AU" term="%22Faudet+A%22">Faudet A</searchLink>; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.<br /><searchLink fieldCode="AU" term="%22Garel+C%22">Garel C</searchLink>; AP-HP GHUEP, Hôpital Armand Trousseau, Service de Radiologie, Paris, France.<br /><searchLink fieldCode="AU" term="%22Gillies+G%22">Gillies G</searchLink>; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Gobius+I%22">Gobius I</searchLink>; Queensland Brain Institute, University of Queensland, St. Lucia, Brisbane, Australia.<br /><searchLink fieldCode="AU" term="%22Guegan+J%22">Guegan J</searchLink>; iCONICS Facility, ICM, Paris, France.<br /><searchLink fieldCode="AU" term="%22Heide+S%22">Heide S</searchLink>; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; Groupe de Recherche Clinique (GRC) `Déficience Intellectuelle et Autisme' UPMC, Paris, France.<br /><searchLink fieldCode="AU" term="%22Keren+B%22">Keren B</searchLink>; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.<br /><searchLink fieldCode="AU" term="%22Lesne+F%22">Lesne F</searchLink>; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.<br /><searchLink fieldCode="AU" term="%22Lukic+V%22">Lukic V</searchLink>; Bioinformatics Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Mandelstam+SA%22">Mandelstam SA</searchLink>; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.; Florey Institute of Neuroscience and Mental Health, Melbourne, Victoria, Australia.; Department of Radiology, University of Melbourne, Royal Children's Hospital, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22McGillivray+G%22">McGillivray G</searchLink>; Victorian Clinical Genetics Services, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22McIlroy+A%22">McIlroy A</searchLink>; Developmental Imaging and Child Neuropsychology Research Groups, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Méneret+A%22">Méneret A</searchLink>; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Neurologie, Paris, France.<br /><searchLink fieldCode="AU" term="%22Mignot+C%22">Mignot C</searchLink>; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; Groupe de Recherche Clinique (GRC) `Déficience Intellectuelle et Autisme' UPMC, Paris, France.; Centre de Référence `Déficiences Intellectuelles de Causes Rares', Paris, France.<br /><searchLink fieldCode="AU" term="%22Morcom+LR%22">Morcom LR</searchLink>; Queensland Brain Institute, University of Queensland, St. Lucia, Brisbane, Australia.<br /><searchLink fieldCode="AU" term="%22Odent+S%22">Odent S</searchLink>; Service de Génétique Clinique, Centre de Référence CLAD-Ouest, CHU Rennes, Rennes, France.; UMR 6290 CNRS, IGDR Institut de Génétique et Développement de Rennes, Université de Rennes 1, Rennes, France.<br /><searchLink fieldCode="AU" term="%22Paolino+A%22">Paolino A</searchLink>; Queensland Brain Institute, University of Queensland, St. Lucia, Brisbane, Australia.<br /><searchLink fieldCode="AU" term="%22Pope+K%22">Pope K</searchLink>; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Riant+F%22">Riant F</searchLink>; AP-HP, Groupe Hospitalier Saint-Louis -La Riboisière -Fernand Vidal, Laboratoire de Génétique, Paris, France.<br /><searchLink fieldCode="AU" term="%22Robinson+GA%22">Robinson GA</searchLink>; Neuropsychology Research Unit, School of Psychology, University of Queensland, Brisbane, Australia.<br /><searchLink fieldCode="AU" term="%22Spencer-Smith+M%22">Spencer-Smith M</searchLink>; Developmental Imaging and Child Neuropsychology Research Groups, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; School of Psychological Sciences and Monash Institute of Cognitive and Clinical Neurosciences, Monash University, Clayton, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Srour+M%22">Srour M</searchLink>; Department of Pediatrics, Montreal Children's Hospital, McGill University, Montreal, Quebec, Canada.; Department of Neurology and Neurosurgery, McGill University Health Center, Montreal, Quebec, Canada.<br /><searchLink fieldCode="AU" term="%22Stephenson+SE%22">Stephenson SE</searchLink>; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Tankard+R%22">Tankard R</searchLink>; Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.; Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Trouillard+O%22">Trouillard O</searchLink>; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.<br /><searchLink fieldCode="AU" term="%22Welniarz+Q%22">Welniarz Q</searchLink>; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.; Institut de Biologie Paris Seine, Neuroscience Paris Seine, Sorbonne Universités, UPMC Univ Paris 06, INSERM, CNRS, Paris, France.<br /><searchLink fieldCode="AU" term="%22Wood+A%22">Wood A</searchLink>; Developmental Imaging and Child Neuropsychology Research Groups, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; School of Life and Health Sciences, Aston University, Birmingham, UK.<br /><searchLink fieldCode="AU" term="%22Brice+A%22">Brice A</searchLink>; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.<br /><searchLink fieldCode="AU" term="%22Rouleau+G%22">Rouleau G</searchLink>; Department of Neurology and Neurosurgery, McGill University Health Center, Montreal, Quebec, Canada.; Montreal Neurological Institute and Hospital, McGill University, Montréal, Quebec, Canada.<br /><searchLink fieldCode="AU" term="%22Attié-Bitach+T%22">Attié-Bitach T</searchLink>; INSERM U1163, Laboratory of Embryology and Genetics of Congenital Malformations, Paris-Descartes University, Sorbonne Paris Cité and Imagine Institute, Paris, France.; AP-HP, Hôpital Necker-Enfants Malades, Département de Génétique, Paris, France.<br /><searchLink fieldCode="AU" term="%22Delatycki+MB%22">Delatycki MB</searchLink>; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Mandel+JL%22">Mandel JL</searchLink>; IGBMC, Université de Strasbourg, CNRS, INSERM, UMR7104 U964, Strasbourg, France.; Laboratoires de Génétique, Institut de Génétique Médicale d'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.<br /><searchLink fieldCode="AU" term="%22Amor+DJ%22">Amor DJ</searchLink>; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Roze+E%22">Roze E</searchLink>; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Neurologie, Paris, France.<br /><searchLink fieldCode="AU" term="%22Piton+A%22">Piton A</searchLink>; IGBMC, Université de Strasbourg, CNRS, INSERM, UMR7104 U964, Strasbourg, France.; Laboratoires de Génétique, Institut de Génétique Médicale d'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.<br /><searchLink fieldCode="AU" term="%22Bahlo+M%22">Bahlo M</searchLink>; Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.; Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Billette+de+Villemeur+T%22">Billette de Villemeur T</searchLink>; Centre de Référence `Déficiences Intellectuelles de Causes Rares', Paris, France.; AP-HP, Hôpital Trousseau, Service de Neuropédiatrie, Paris, France.; UPMC, GRC ConCer-LD, Sorbonne Université, Paris, France.; INSERM U1141, Paris, France.<br /><searchLink fieldCode="AU" term="%22Sherr+EH%22">Sherr EH</searchLink>; Department of Neurology, UCSF Benioff Children's Hospital, San Francisco, California, USA.<br /><searchLink fieldCode="AU" term="%22Leventer+RJ%22">Leventer RJ</searchLink>; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.; Neuroscience Research Group, Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; Department of Neurology, University of Melbourne, Royal Children's Hospital, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Richards+LJ%22">Richards LJ</searchLink>; Queensland Brain Institute, University of Queensland, St. Lucia, Brisbane, Australia.; University of Queensland, School of Biomedical Sciences, St. Lucia, Brisbane, Australia.<br /><searchLink fieldCode="AU" term="%22Lockhart+PJ%22">Lockhart PJ</searchLink>; Bruce Lefroy Centre for Genetic Health Research, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Depienne+C%22">Depienne C</searchLink>; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; IGBMC, Université de Strasbourg, CNRS, INSERM, UMR7104 U964, Strasbourg, France.; INSERM, U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.; Laboratoires de Génétique, Institut de Génétique Médicale d'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
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  Data: <searchLink fieldCode="JN" term="%229216904%22">Nature genetics</searchLink> [Nat Genet] 2017 Apr; Vol. 49 (4), pp. 511-514. <i>Date of Electronic Publication: </i>2017 Feb 27.
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      – TitleFull: Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance.
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            NameFull: Billette de Villemeur T
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            – D: 01
              M: 04
              Text: 2017 Apr
              Type: published
              Y: 2017
          Identifiers:
            – Type: issn-electronic
              Value: 1546-1718
          Numbering:
            – Type: volume
              Value: 49
            – Type: issue
              Value: 4
          Titles:
            – TitleFull: Nature genetics
              Type: main
ResultId 1