Authors: Rong Weining, Zou Gang, Sheng Xunlun, Li Huiping, Zhang Fangxia DOI: 10.3760/cma.j.issn.2095-0160.2015.08.010 Published 2015-08-10 Cite as Chin J Exp Ophthalmol, 2015,33(8): 711-715. Abstract [Download PDF] [Read Full Text] Background Congenital cataract is an important cause of blindness and amblyopia in children, […]
Tag: Cataract/genetics
A recurrent mutation of CRYGD gene in a northern Chinese family with autosomal dominant congenital nuclear cataract
Authors: Zhang Xiaohui, Liu Weihua, Dong Bing, Chen Jieqiong, Li Yang DOI: 10.3760/cma.j.issn.2095-0160.2015.08.012 Published 2015-08-10 Cite as Chin J Exp Ophthalmol, 2015,33(8): 722-726. Abstract [Download PDF] [Read Full Text] Background Congenital cataract is a major cause for blindness of childhood. Genetic […]
Analysis of GJA3 mutation associated with a Chinese family with autosomal dominant congenital cataract by whole-exome sequencing
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 […]