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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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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Autosomal Dominant Congenital Nuclear Cataracts Caused by a CRYAA Gene Mutation

By Li Fei-Feng   Yang Min   Ma Xu   Zhang Qiong   Zhang Meng   Wang Shu-Zhen   Zhu Si-Quan  

Current Eye Research, Vol. 35, Iss. 6, 2010-06 ,pp. : 492-498

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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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Progressive autosomal dominant optic atrophy and sensorineural hearing loss in a Turkish family

By Özden Serap   Düzcan Füsun   Wollnik Bernd   Çetin G. Ozan   Sahiner Türker   Bayramoglu Ismet   Yüksel-Apak Memnune   Bagci Hüseyin  

Ophthalmic Genetics, Vol. 23, Iss. 1, 2002-03 ,pp. : 29-36

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