Mutations in a new photoreceptor-pineal gene on 17p cause leber congenital amaurosis. Nat gen 2000;24:79-83
17p染色体上一个新的光感受器-松果体基因的突变导致莱伯氏先天性黑蒙症。Nat gen 2000;24:79-83
期刊:American Journal of Ophthalmology
影响因子:4.2
doi:10.1016/s0002-9394(00)00517-1
Sohoki, MM; Browne, SJ; Sullivan, LS; Blackshaw, S; Cepko, CL; Payne, AM; Bhattacharya, SS; Khaliq, S; Mehdi, SQ; Birch, DG; Harrison, WR; Elder, FF; Heckenlively, JR; Daiger, SP
