A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital Cataract

Open Access

Peer-reviewed

Research Article

Yanan Zhu,

Affiliations Eye center, 2nd Affiliated Hospital of Medical College, Zhejiang University, Hangzhou, China, Key Laboratory of Ophthalmology of Zhejiang Province, Wenzhou, China
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Hao Yu,

Affiliation Department of Neurobiology, Key Laboratory of Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, Hangzhou, China
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Wei Wang,

Affiliations Eye center, 2nd Affiliated Hospital of Medical College, Zhejiang University, Hangzhou, China, Key Laboratory of Ophthalmology of Zhejiang Province, Wenzhou, China
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Xiaohua Gong,

Affiliation School of Optometry and Vision Science Program, University of California, Berkeley, California, United States of America
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Ke Yao

* E-mail: xlren@zju.edu.cn

Affiliations Eye center, 2nd Affiliated Hospital of Medical College, Zhejiang University, Hangzhou, China, Key Laboratory of Ophthalmology of Zhejiang Province, Wenzhou, China
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Cataracts
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Gap junctions
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Transfection
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HeLa cells
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Mutation detection
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Cataract surgery
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Mutation
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Valine
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