Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm.

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Bibliographic Details
Title: Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm.
Authors: Chetaille P; Department of Pediatrics, Centre Mère Enfants Soleil, Centre Hospitalier de l'Université (CHU) de Québec, Quebec City, Quebec, Canada., Preuss C; Cardiovascular Genetics, Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine Research Centre, Université de Montréal, Montreal, Quebec, Canada., Burkhard S; Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences (KNAW) and University Medical Center Utrecht, Utrecht, the Netherlands., Côté JM; Department of Pediatrics, Centre Mère Enfants Soleil, Centre Hospitalier de l'Université (CHU) de Québec, Quebec City, Quebec, Canada., Houde C; Department of Pediatrics, Centre Mère Enfants Soleil, Centre Hospitalier de l'Université (CHU) de Québec, Quebec City, Quebec, Canada., Castilloux J; Department of Pediatrics, Centre Mère Enfants Soleil, Centre Hospitalier de l'Université (CHU) de Québec, Quebec City, Quebec, Canada., Piché J; Cardiovascular Genetics, Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine Research Centre, Université de Montréal, Montreal, Quebec, Canada., Gosset N; Cardiovascular Genetics, Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine Research Centre, Université de Montréal, Montreal, Quebec, Canada., Leclerc S; Cardiovascular Genetics, Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine Research Centre, Université de Montréal, Montreal, Quebec, Canada., Wünnemann F; Cardiovascular Genetics, Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine Research Centre, Université de Montréal, Montreal, Quebec, Canada., Thibeault M; Cardiovascular Genetics, Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine Research Centre, Université de Montréal, Montreal, Quebec, Canada., Gagnon C; Cardiovascular Genetics, Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine Research Centre, Université de Montréal, Montreal, Quebec, Canada., Galli A; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, UK., Tuck E; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, UK., Hickson GR; Department of Pediatrics, Université de Montréal, Montreal, Quebec, Canada., El Amine N; Department of Pediatrics, Université de Montréal, Montreal, Quebec, Canada., Boufaied I; Department of Pediatrics, Université de Montréal, Montreal, Quebec, Canada., Lemyre E; Department of Pediatrics, Université de Montréal, Montreal, Quebec, Canada., de Santa Barbara P; INSERM U1046, Montpellier, France., Faure S; INSERM U1046, Montpellier, France., Jonzon A; Department of Women's and Children's Health, Section for Pediatrics, Astrid Lindgren's Children's Hospital, Uppsala University, Uppsala, Sweden., Cameron M; Cardiovascular Genetics, Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine Research Centre, Université de Montréal, Montreal, Quebec, Canada., Dietz HC; Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Gallo-McFarlane E; Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Benson DW; Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin, USA., Moreau C; Department of Pediatrics, Université de Montréal, Montreal, Quebec, Canada., Labuda D; Department of Pediatrics, Université de Montréal, Montreal, Quebec, Canada., Zhan SH; Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, British Columbia, Canada., Shen Y; Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, British Columbia, Canada., Jomphe M; Projet BALSAC, Université du Québec à Chicoutimi, Chicoutimi, Quebec, Canada., Jones SJ; Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, British Columbia, Canada., Bakkers J; Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences (KNAW) and University Medical Center Utrecht, Utrecht, the Netherlands., Andelfinger G; 1] Cardiovascular Genetics, Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine Research Centre, Université de Montréal, Montreal, Quebec, Canada. [2] Department of Pediatrics, Université de Montréal, Montreal, Quebec, Canada. [3] Department of Biochemistry, Université de Montréal, Montreal, Quebec, Canada.
Corporate Authors: FORGE Canada Consortium
Source: Nature genetics [Nat Genet] 2014 Nov; Vol. 46 (11), pp. 1245-9. Date of Electronic Publication: 2014 Oct 05.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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
Database: MEDLINE Ultimate
Description
ISSN:1546-1718
DOI:10.1038/ng.3113