NR2F1 Mutations Cause Optic Atrophy with Intellectual Disability
2014; Elsevier BV; Volume: 94; Issue: 2 Linguagem: Inglês
10.1016/j.ajhg.2014.01.002
ISSN1537-6605
AutoresDaniëlle G.M. Bosch, F. Nienke Boonstra, Claudia Gonzaga‐Jauregui, Mafei Xu, Joep de Ligt, Shalini N. Jhangiani, Wojciech Wiszniewski, Donna M. Muzny, Helger G. Yntema, Rolph Pfundt, Lisenka E.L.M. Vissers, Liesbeth Spruijt, Ellen A.W. Blokland, Chun‐An Chen, Richard A. Lewis, Sophia Y. Tsai, Richard A. Gibbs, Ming‐Jer Tsai, James R. Lupski, Huda Y. Zoghbi, Frans P.M. Cremers, Bert B.A. de Vries, Christian P. Schaaf,
Tópico(s)Ubiquitin and proteasome pathways
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