Tag: Amino Acid Sequence

Analysis of GJA3 mutation associated with a Chinese family with autosomal dominant congenital cataract by whole-exome sequencing

2016, No. 10, Clinical Science

Authors：Liu Yuying,  Wan Wencui,  Yang Ge,  Pang Xuena,  Yang Guoguo,  Jin Xuemin DOI: 10.3760/cma.j.issn.2095-0160.2016.10.011 Published 2016-10-10 Cite as Chin J Exp Ophthalmol, 2016,34(10): 916-919. Abstract                              [Download PDF] [Read Full Text] Congenital cataract is one of the important reasons for the blindness of children, and most congenital […]