A deletion mutation in the ?A1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family

Yanhua Qi(Harbin Medical University), Ying Li(Eli Lilly (United States)), Hong Su(Anhui University of Science and Technology), Shangzhi Huang(Peking Union Medical College Hospital), Lijun Qu(Harbin Medical University), Dandan Li(Guangdong Ocean University), Hongyan Jia(Capital Medical University), Hui Lin(Harbin Medical University), Ya Gao(BGI Group (China)), Jing-zhi Gu(Harbin Medical University), Tieying Zhang(Shihezi University)
Human Genetics
January 1, 2004
10.1007/s00439-003-1049-7
Cited by 69

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