A novel missense SNRNP200 mutation associated with autosomal dominant retinitis pigmentosa in a Chinese family.

Por Tiecheng Liu, Xin Jin, Xuemin Zhang, Huijun Yuan, Jing Cheng, Janet Lee, Baoquan Zhang, Maonian Zhang, Jing Wu, Lijuan Wang, Geng Tian, Weifeng Wang
Publicado em 2012-01-01