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Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study.
Hardcastle, A J; Thiselton, D L; Van Maldergem, L; Saha, B K; Jay, M; Plant, C; Taylor, R; Bird, A C; Bhattacharya, S.
Am J Hum Genet ; 64(4): 1210-5, 1999 Apr.
Article in En | MEDLINE | ID: mdl-10090907
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Proteins / Retinitis Pigmentosa / Eye Proteins / Genetic Linkage / Mutation Limits: Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 1999 Document type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Proteins / Retinitis Pigmentosa / Eye Proteins / Genetic Linkage / Mutation Limits: Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 1999 Document type: Article