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Characterization of Loss-Of-Function KCNJ2 Mutations in Atypical Andersen Tawil Syndrome.

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Title: Characterization of Loss-Of-Function KCNJ2 Mutations in Atypical Andersen Tawil Syndrome.
Authors: Le Tanno P; Université Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, Grenoble, France., Folacci M; CEA, CNRS, Institut de Biologie Structurale, Université Grenoble Alpes, Grenoble, France., Revilloud J; CEA, CNRS, Institut de Biologie Structurale, Université Grenoble Alpes, Grenoble, France., Faivre L; Medical Genetics Department, Dijon Bourgogne University Hospital, François Mitterand Hospital, Dijon, France., Laurent G; Cardiology Department, Dijon Bourgogne University Hospital, François Mitterand Hospital, Dijon, France., Pinson L; Medical Genetics Department, University Hospital, Montpellier, France.; Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Montpellier, France.; Genetic Department for Rare Diseases and Personalized Medicine, Clinical Division, Montpellier, France., Amedro P; Pediatric and Congenital Cardiology Department, Clinical Investigation Centre, PhyMedExp, CNRS, INSERM, University of Montpellier, University Hospital, Montpellier, France., Millat G; Laboratoire de Cardiogénétique Moléculaire, Centre de Biologie et Pathologie Est, Hospices Civils de Lyon, Lyon, France., Janin A; Laboratoire de Cardiogénétique Moléculaire, Centre de Biologie et Pathologie Est, Hospices Civils de Lyon, Lyon, France., Vivaudou M; CEA, CNRS, Institut de Biologie Structurale, Université Grenoble Alpes, Grenoble, France., Roux-Buisson N; Université Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, Grenoble, France., Fauré J; Université Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, Grenoble, France.
Source: Frontiers in genetics [Front Genet] 2021 Nov 25; Vol. 12, pp. 773177. Date of Electronic Publication: 2021 Nov 25 (Print Publication: 2021).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE
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  Data: Characterization of Loss-Of-Function KCNJ2 Mutations in Atypical Andersen Tawil Syndrome.
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  Data: <searchLink fieldCode="AU" term="%22Le+Tanno+P%22">Le Tanno P</searchLink>; Université Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, Grenoble, France.<br /><searchLink fieldCode="AU" term="%22Folacci+M%22">Folacci M</searchLink>; CEA, CNRS, Institut de Biologie Structurale, Université Grenoble Alpes, Grenoble, France.<br /><searchLink fieldCode="AU" term="%22Revilloud+J%22">Revilloud J</searchLink>; CEA, CNRS, Institut de Biologie Structurale, Université Grenoble Alpes, Grenoble, France.<br /><searchLink fieldCode="AU" term="%22Faivre+L%22">Faivre L</searchLink>; Medical Genetics Department, Dijon Bourgogne University Hospital, François Mitterand Hospital, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Laurent+G%22">Laurent G</searchLink>; Cardiology Department, Dijon Bourgogne University Hospital, François Mitterand Hospital, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Pinson+L%22">Pinson L</searchLink>; Medical Genetics Department, University Hospital, Montpellier, France.; Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Montpellier, France.; Genetic Department for Rare Diseases and Personalized Medicine, Clinical Division, Montpellier, France.<br /><searchLink fieldCode="AU" term="%22Amedro+P%22">Amedro P</searchLink>; Pediatric and Congenital Cardiology Department, Clinical Investigation Centre, PhyMedExp, CNRS, INSERM, University of Montpellier, University Hospital, Montpellier, France.<br /><searchLink fieldCode="AU" term="%22Millat+G%22">Millat G</searchLink>; Laboratoire de Cardiogénétique Moléculaire, Centre de Biologie et Pathologie Est, Hospices Civils de Lyon, Lyon, France.<br /><searchLink fieldCode="AU" term="%22Janin+A%22">Janin A</searchLink>; Laboratoire de Cardiogénétique Moléculaire, Centre de Biologie et Pathologie Est, Hospices Civils de Lyon, Lyon, France.<br /><searchLink fieldCode="AU" term="%22Vivaudou+M%22">Vivaudou M</searchLink>; CEA, CNRS, Institut de Biologie Structurale, Université Grenoble Alpes, Grenoble, France.<br /><searchLink fieldCode="AU" term="%22Roux-Buisson+N%22">Roux-Buisson N</searchLink>; Université Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, Grenoble, France.<br /><searchLink fieldCode="AU" term="%22Fauré+J%22">Fauré J</searchLink>; Université Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, Grenoble, France.
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