Novel BEST1 mutations and special clinical characteristics of autosomal recessive bestrophinopathy in Chinese patients.
Luo J, Lin M, Guo X, Xiao X, Li J, Hu H, Xiao H, Xu X, Zhong Y, Long S, Luo G, Mi L, Chen X, Fang L, Wei W, Zhang Q, Liu X.
Luo J, et al. Among authors: zhong y.
Acta Ophthalmol. 2019 May;97(3):247-259. doi: 10.1111/aos.13994. Epub 2018 Dec 28.
Acta Ophthalmol. 2019.
PMID: 30593719
Free article.