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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Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the family

By Van Ghelue Marijke   Eriksen Hans L.   Ponjavic Vesna   Fagerheim Toril   Andréasson Sten   Forsman-Semb Kristina   Sandgren Ola   Holmgren Gösta   Tranebjærg Lisbeth  

Ophthalmic Genetics, Vol. 21, Iss. 4, 2000-12 ,pp. : 197-209

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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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