LCA5, a Rare Genetic Cause of Leber Congenital Amaurosis in Koreans

By Seong Moon-Woo   Kim Seong Yeon   Yu Young Suk   Hwang Jeong-Min   Kim Ji Yeon   Park Sung Sup  

Ophthalmic Genetics, Vol. 30, Iss. 1, 2009-03 ,pp. : 54-55

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Genetic Screening of Leber Congenital Amaurosis in a Large Consanguineous Iranian Family

By Rezaie Tayebeh   Karimi-Nejad Mohammad-Hassan   Meshkat Mohammad-Reza   Sohbati Saeed   Karimi-Nejad Roxana   Najmabadi Hossein   Sarfarazi Mansoor  

Ophthalmic Genetics, Vol. 28, Iss. 4, 2007-10 ,pp. : 224-228

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Agenesis of the corpus callosum in a child with Leber's congenital amaurosis

By Kiratli Hayyam   Tatlipinar Sinan  

Ophthalmic Genetics, Vol. 20, Iss. 3, 1999-09 ,pp. : 183-187

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Mutational analysis and clinical correlation in Leber congenital amaurosis

By Dharmaraj Sharola   Silva Eduardo   Pina Ana Luisa   Li Ying Ying   Yang Jun-Ming   Carter R. Colin   Loyer Magali   El-Hilali Hala   Traboulsi Elias   Sundin Olof   Zhu Danping   Koenekoop Robert K.   Maumenee Irene H.  

Ophthalmic Genetics, Vol. 21, Iss. 3, 2000-09 ,pp. : 135-150

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Visual improvement in Leber congenital amaurosis and the CRX genotype

By Koenekoop Robert K.   Loyer Magali   Dembinska Olga   Beneish Raquel  

Ophthalmic Genetics, Vol. 23, Iss. 1, 2002-03 ,pp. : 49-59

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