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

By Andréasson Sten   Breuer Debra K.   Eksandh Louise   Ponjavic Vesna   Frennesson Christina   Hiriyanna Suja   Filippova Elena   Yashar Beverly M.   Swaroop Anand  

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

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Novel deletion of the RPGR gene in a Chinese family with X-linked retinitis pigmentosa

By Zhao Kanxing   Wang Lejin   Wang Li   Wang Liming   Zhang Qingsheng   Wang Qing  

Ophthalmic Genetics, Vol. 22, Iss. 3, 2001-09 ,pp. : 187-194

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Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2)

By Rosenberg Thomas   Schwahn Uwe   Feil Silke   Berger Wolfgang  

Ophthalmic Genetics, Vol. 20, Iss. 3, 1999-09 ,pp. : 161-172

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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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Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype

By Ponjavic Vesna   Andréasson Sten   Abrahamson Magnus   Ehinger Berndt   Gieser Linn   Fujita Ricardo   Swaroop Anand   Swaroop Anand  

Ophthalmic Genetics, Vol. 19, Iss. 4, 1998-12 ,pp. : 187-196

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