Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus. | Hum Genet;105(1-2): 57-62, 1999. | MEDLINE

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Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus.

Zito, I; Thiselton, D L; Gorin, M B; Stout, J T; Plant, C; Bird, A C; Bhattacharya, S S; Hardcastle, A J.

Affiliation

Zito I; Department of Molecular Genetics, Institute of Ophthalmology, University College London, UK.

Hum Genet ; 105(1-2): 57-62, 1999.

Article in En | MEDLINE | ID: mdl-10480356

Subject(s)

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Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Proteins / Carrier Proteins / Retinitis Pigmentosa / Frameshift Mutation / Eye Proteins / Genetic Linkage Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Hum Genet Year: 1999 Document type: Article Affiliation country:

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Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Proteins / Carrier Proteins / Retinitis Pigmentosa / Frameshift Mutation / Eye Proteins / Genetic Linkage Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Hum Genet Year: 1999 Document type: Article Affiliation country: