A deletion mutation in the βA1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family

Author: Qi Yanhua   Jia Hongyan   Huang Shangzhi   Lin Hui   Gu Jingzhi   Su Hong   Zhang Tieying   Gao Ya   Qu Lijun   Li Dandan   Li Ying  

Publisher: Springer Publishing Company

ISSN: 0340-6717

Source: Human Genetics, Vol.114, Iss.2, 2004-01, pp. : 192-197

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