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  • Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia

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Developmental defects
Original article
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia

Authors

  • Mark E Samuels Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Jacek Majewski Department of Human Genetics, McGill University, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Najmeh Alirezaie Department of Human Genetics, McGill University, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Isabel Fernandez Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, CanadaDepartment of Microbiology and Immunology, University of Montreal, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Ferran Casals Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Natalie Patey Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, CanadaDepartment of Pathology, University of Montreal, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Hélène Decaluwe Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, CanadaDepartment of Pediatrics, University of Montreal, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Isabelle Gosselin Department of Neurosciences, Centre de recherche du CHU de Québec, Université Laval, Québec City, Quebec, Canada PubMed articlesGoogle scholar articles
  • Elie Haddad Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, CanadaDepartment of Microbiology and Immunology, University of Montreal, Montreal, Quebec, CanadaDepartment of Pediatrics, University of Montreal, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Alan Hodgkinson Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Youssef Idaghdour Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Valerie Marchand Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, CanadaDepartment of Pediatrics, University of Montreal, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Jacques L Michaud Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, CanadaDepartment of Pediatrics, University of Montreal, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Marc-André Rodrigue Department of Neurosciences, Centre de recherche du CHU de Québec, Université Laval, Québec City, Quebec, CanadaDépartement de Médecine Moléculaire, Université Laval, Québec City, Quebec, Canada PubMed articlesGoogle scholar articles
  • Sylvie Desjardins Department of Neurosciences, Centre de recherche du CHU de Québec, Université Laval, Québec City, Quebec, Canada PubMed articlesGoogle scholar articles
  • Stéphane Dubois Department of Neurosciences, Centre de recherche du CHU de Québec, Université Laval, Québec City, Quebec, Canada PubMed articlesGoogle scholar articles
  • Francoise Le Deist Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, CanadaDepartment of Microbiology and Immunology, University of Montreal, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Philip Awadalla Centre de Recherche du CHU Ste-Justine, University of Montreal, Montreal, Quebec, CanadaDepartment of Pediatrics, University of Montreal, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Vincent Raymond Department of Neurosciences, Centre de recherche du CHU de Québec, Université Laval, Québec City, Quebec, CanadaDépartement de Médecine Moléculaire, Université Laval, Québec City, Quebec, Canada PubMed articlesGoogle scholar articles
  • Bruno Maranda Medical Genetics Service, University of Sherbrooke, Sherbrooke, Quebec, Canada PubMed articlesGoogle scholar articles
  1. Correspondence to Bruno Maranda, Medical Genetics Service, University of Sherbrooke, Sherbrooke, Quebec, Canada J1K 2R1; Bruno.Maranda{at}USherbrooke.ca
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Citation

Samuels ME, Majewski J, Alirezaie N, et al
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia
Journal of Medical Genetics 2013;50:324-329.

Publication history

  • Received December 14, 2012
  • Accepted January 22, 2013
  • First published February 19, 2013.
Online issue publication 
July 29, 2016

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