A R54L Mutation of CRYAA Associated with Autosomal Dominant Nuclear Cataracts in a Chinese Family

By Yang Zhenfei   Su Dongmei   Li Qian   Ma Zicheng   Yang Fan   Zhu Siquan   Ma Xu  

Current Eye Research, Vol. 38, Iss. 12, 2013-12 ,pp. : 1221-1228

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A Novel Mutation in the Connexin 50 Gene (GJA8) Associated with Autosomal Dominant Congenital Nuclear Cataract in a Chinese Family

By Gao Xiaobo   Cheng Jie   Lu Cailing   Li Xiaoqiao   Li Feifeng   Liu Chunmei   Zhang Meng   Zhu Siquan   Ma Xu  

Current Eye Research, Vol. 35, Iss. 7, 2010-07 ,pp. : 597-604

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Evidence of clinical and genetic heterogeneity in autosomal dominant congenital cerulean cataracts

By Hilal Latifa   Nandrot Emeline   Belmekki Mohamed   Chefchaouni Mohamed   Bacha Siham El   Benazzouz Bouchra   Hajaji Yassir   Gribouval Olivier   Dufier Jean-Louis   Abitbol Marc   Berraho Amina  

Ophthalmic Genetics, Vol. 23, Iss. 4, 2002-12 ,pp. : 199-208

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A Novel CRYBB2 Missense Mutation Causing Congenital Autosomal Dominant Cataract in an Italian Family

By Faletra Flavio   d'Adamo Adamo Pio   Pensiero Stefano   Athanasakis Emmanouil   Catalano Dario   Bruno Irene   Gasparini Paolo  

Ophthalmic Genetics, Vol. 34, Iss. 1-2, 2013-06 ,pp. : 115-117

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Further Genetic Heterogeneity for Autosomal Dominant Human Sutural Cataracts

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Ophthalmic Research, Vol. 35, Iss. 2, 2003-03 ,pp. : 71-77

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