Novel variants of ABCA4 in Han Chinese families with Stargardt disease
Stargardt disease (STGD1) is a common recessive hereditary macular dystrophy in early adulthood or childhood, with an estimated prevalence of 1:8000 to 1:10,000. ABCA4 is the causative gene for STGD1. The current...
Source: BMC Medical Genetics - Category: Genetics & Stem Cells Authors: Fang-Yuan Hu, Feng-Juan Gao, Jian-kang Li, Ping Xu, Dan-Dan Wang, Sheng-Hai Zhang and Ji-Hong Wu Tags: Research article Source Type: research