Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes

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Ophthalmic Genetics, Vol. 24, Iss. 4, 2003-12 ,pp. : 215-223

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Mutations in RPGR and RP2 of Chinese Patients with X-Linked Retinitis Pigmentosa

By Ji Yanli   Wang Juan   Xiao Xueshan   Li Shiqiang   Guo Xiangming   Zhang Qingjiong  

Current Eye Research, Vol. 35, Iss. 1, 2010-01 ,pp. : 73-79

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Phenotype associated with an R120X nonsense mutation in the RP2 gene in a Japanese family with X-linked retinitis pigmentosa

By Mashima Yukihiko   Saga Masamichi   Akeo Kiyoshi   Oguchi Yoshihisa  

Ophthalmic Genetics, Vol. 22, Iss. 1, 2001-03 ,pp. : 43-47

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Phenotype Associated with the H626P Mutation and Other Changes in the TGFBI Gene in Czech Families

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Ophthalmic Research, Vol. 40, Iss. 2, 2008-02 ,pp. : 105-108

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A correlation between computer-predicted changes in secondary structure and the phenotype of retinal degeneration associated with mutations in peripherin/RDS

By Nakazawa Mitsuru   Wada Yuko   Chida Yasushi   Tamai Makoto  

Current Eye Research, Vol. 16, Iss. 11, 1997-11 ,pp. : 1134-1141

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