Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism
Christian P. Schaaf(Baylor College of Medicine), Manuel L. Gonzalez‐Garay(Brown Foundation), Fan Xia(Baylor College of Medicine), Lorraine Potocki(Baylor College of Medicine), Karen W. Gripp(Alfred I. duPont Hospital for Children), Baili Zhang(Baylor College of Medicine), Brock A. Peters(Complete Genomics (United States)), Mark A. McElwain(Complete Genomics (United States)), Radoje Drmanac(Complete Genomics (United States)), Arthur L. Beaudet(Baylor College of Medicine), C. Thomas Caskey(Baylor College of Medicine), Yaping Yang(Baylor College of Medicine)
Cited by 303Open Access