Yang, G., Zhai, X., & Zhao, J. (2011). A recurrent mutation in CRYBA1 is associated with an autosomal dominant congenital nuclear cataract disease in a Chinese family. Molecular Vision.
Chicago-stil citatYang, Guoxing, Xinling Zhai, och Jialiang Zhao. A Recurrent Mutation in CRYBA1 Is Associated With an Autosomal Dominant Congenital Nuclear Cataract Disease in a Chinese Family. Molecular Vision, 2011.
MLA-referensYang, Guoxing, Xinling Zhai, och Jialiang Zhao. A Recurrent Mutation in CRYBA1 Is Associated With an Autosomal Dominant Congenital Nuclear Cataract Disease in a Chinese Family. Molecular Vision, 2011.
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