Tag: pair 11/genetics

A novel PAX6 mutation in a Chinese family with congenital aniridia

2016, No. 07, Clinical Science

Authors: Liu Yuying,  Liu Qiong,  Wan Wencui,  Yang Ge,  Xia Kun,  Jin Xuemin DOI: 10.3760/cma.j.issn.2095-0160.2016.07.006 Published 2016-07-10 Cite as Chin J Exp Ophthalmol, 2016,34(7): 602-606. Abstract                               [Download PDF] [Read Full Text] Background Aniridia is a rare congenital hereditary eye disease.Studies determined that PAX6 gene mutation is closely associated […]

Genetic analysis of a Chinese family with congenital aniridia and detection of PAX6 mutation locus

2017, No. 08, Clinical Science

Authors: Zhang Luxi,  Yang Ge,  Jia Jing,  Wan Wencui,  Yang Xin,  Jin Xuemin DOI: 10.3760/cma.j.issn.2095-0160.2017.08.011 Published 2017-08-10 Cite as Chin J Exp Ophthalmol, 2017,35(8): 721-725. Abstract                               [Download PDF] [Read Full Text] Background Congenital aniridia is a rare bilateral hereditary ophthalmopathy which impact panocular.Researches showed that congenital aniridia can be caused by […]