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

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

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

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

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

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