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A Framework to Identify Contributing Genes in Patients with Phelan-Mcdermid Syndrome

Anne-Claude Tabet,Thomas Rolland,Marie Ducloy,Jonathan Lévy,Julien Buratti,Alexandre Mathieu,Damien Haye,Laurence Perrin,Céline Dupont,Sandrine Passemard,Yline Capri,Alain Verloes,Séverine Drunat,Boris Keren,Cyril Mignot,Isabelle Marey,Aurélia Jacquette,Sandra Whalen,Eva Pipiras,Brigitte Benzacken,Sandra Chantot-Bastaraud,Alexandra Afenjar,Delphine Héron,Cédric Le Caignec,Claire Beneteau,Olivier Pichon,Bertrand Isidor,Albert David,Laila El Khattabi,Stephan Kemeny,Laetitia Gouas,Philippe Vago,Anne-Laure Mosca-Boidron,Laurence Faivre,Chantal Missirian,Nicole Philip,Damien Sanlaville,Patrick Edery,Véronique Satre,Charles Coutton,Françoise Devillard,Klaus Dieterich,Marie-Laure Vuillaume,Caroline Rooryck,Didier Lacombe,Lucile Pinson,Vincent Gatinois,Jacques Puechberty,Jean Chiesa,James Lespinasse,Christèle Dubourg,Chloé Quelin,Mélanie Fradin,Hubert Journel,Annick Toutain,Dominique Martin, Abdelamdjid Benmansour,Claire S. Leblond,Roberto Toro,Frédérique Amsellem,Richard Delorme,Thomas Bourgeron

npj genomic medicine（2017）

Cited 59|Views45
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Key words
Clinical genetics,Neurodevelopmental disorders,Biomedicine,general,Human Genetics,Internal Medicine,Bioinformatics,Gene Therapy,Gene Function
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