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NR2F1 Mutations Cause Optic Atrophy with Intellectual Disability

✍ Scribed by Bosch, Daniëlle G.M.; Boonstra, F. Nienke; Gonzaga-Jauregui, Claudia; Xu, Mafei; de Ligt, Joep; Jhangiani, Shalini; Wiszniewski, Wojciech; Muzny, Donna M.; Yntema, Helger G.; Pfundt, Rolph; Vissers, Lisenka E.L.M.; Spruijt, Liesbeth; Blokland, Ellen A.W.; Chen, Chun-An; Lewis, Richard A.; Tsai, Sophia Y.; Gibbs, Richard A.; Tsai, Ming-Jer; Lupski, James R.; Zoghbi, Huda Y.; Cremers, Frans P.M.; de Vries, Bert B.A.; Schaaf, Christian P.

Book ID: 125444724
Publisher: American Society of Human Genetics
Year: 2014
Tongue: English
Weight: 828 KB
Volume: 94
Category: Article
ISSN: 0002-9297
DOI: 10.1016/j.ajhg.2014.01.002

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