Functional characterization of a novel GUCA1A missense mutation (D144G) in autosomal dominant cone dystrophy: A novel pathogenic GUCA1A variant in COD

por Tang, Suzhen, Xia, Yujun, Dai, Yunhai, Liu, Yaning, Li, Jingshuo, Pan, Xiaojing, Chen, Peng
Publicado 2019