Different functional outcome of RetGC1 and RPE65 gene mutations in Leber congenital amaurosis.

Por Perrault, I, Rozet, J M, Ghazi, I, Leowski, C, Bonnemaison, M, Gerber, S, Ducroq, D, Cabot, A, Souied, E, Dufier, J L, Munnich, A, Kaplan, J
Publicado em 1999