Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism

Christian P. Schaaf(University of Cologne), Yaping Yang(Baylor College of Medicine), Fan Xia(Baylor Genetics), Lorraine Potocki(Texas Children's Hospital), Brock A. Peters(Complete Genomics (United States)), Radoje Drmanac(Complete Genomics (United States)), Karen W. Gripp(Alfred I. duPont Hospital for Children), Arthur L. Beaudet(Lunar and Planetary Institute), Manuel L. Gonzalez‐Garay(Brown Foundation), Baili Zhang(Baylor College of Medicine), C. Thomas Caskey(Baylor College of Medicine), Mark A. McElwain(Stanford University)
Nature Genetics
September 29, 2013
10.1038/ng.2776
Cited by 304

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