论文信息 - PRPH2 mutation as the cause of various clinical manifestations in a family affected with inherited retinal dystrophy - 字舞流文

PRPH2 mutation as the cause of various clinical manifestations in a family affected with inherited retinal dystrophy

H. Ahmadieh | N. Daftarian | Hamideh Sabbaghi | Fatemeh Suri | M. Mirrahimi | Afrooz Moghadasi | Niloufar Zal | Hossein Dehghan Banadaki