Two interactive genes responsible for a new inherited cataract (RCT) in the mouse

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Mammalian Genome, Vol. 12, Iss. 4, 2001-04 ,pp. : 278-283

Springer Publishing Company

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Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract

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Human Molecular Genetics, Vol. 13, Iss. 9, 2004-05 ,pp. : 945-953

Oxford University Press

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Linkage of Polymorphic Congenital Cataract to the γ-Crystallin Gene Locus on Human Chromosome 2q33–35

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Human Molecular Genetics, Vol. 5, Iss. 5, 1996-01 ,pp. : 699-703

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Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA

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Oxford University Press

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

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

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

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