Autosomal Dominant Congenital Nuclear Cataracts Caused by a CRYAA Gene Mutation

By Li Fei-Feng   Yang Min   Ma Xu   Zhang Qiong   Zhang Meng   Wang Shu-Zhen   Zhu Si-Quan  

Current Eye Research, Vol. 35, Iss. 6, 2010-06 ,pp. : 492-498

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A Novel Mutation in the Connexin 50 Gene (GJA8) Associated with Autosomal Dominant Congenital Nuclear Cataract in a Chinese Family

By Gao Xiaobo   Cheng Jie   Lu Cailing   Li Xiaoqiao   Li Feifeng   Liu Chunmei   Zhang Meng   Zhu Siquan   Ma Xu  

Current Eye Research, Vol. 35, Iss. 7, 2010-07 ,pp. : 597-604

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Autosomal-Dominant Cerulean Cataract in a Chinese Family Associated with Gene Conversion Mutation in Beta-B2-Crystallin

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Ophthalmic Research, Vol. 41, Iss. 3, 2009-03 ,pp. : 148-153

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Novel rhodopsin mutation in a Chinese family with autosomal dominant retinitis pigmentosa

By Zhao Kanxing   Xiong Shihong   Wang Li   Wang Lejin   Cui Yun   Wang Qing  

Ophthalmic Genetics, Vol. 22, Iss. 3, 2001-09 ,pp. : 155-162

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Cerebrotendinous Xanthomatosis (CTX): An Association of Pulverulent Cataracts and Pseudo-Dominant Developmental Delay in a Family with a Splice Site Mutation in CYP27A1— A Case Report

By Bourkiza Rabia   Joyce Sarah   Patel Himanshu   Chan Michelle   Meyer Esther   Maher Eamonn R.   Reddy M. Ashwin  

Ophthalmic Genetics, Vol. 31, Iss. 2, 2010-06 ,pp. : 73-76

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