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Article

A family with RP3 type of X-linked retinitis pigmentosa: an association with ciliary abnormalities

1 Jan 1992

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Identifiers

PMID: 1733835
DOI: 10.1007/bf00197269

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Related research

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Click a neighbor to travelStep 1 · 12 closest

A family with RP3 type of X-linked retinitis pigmentosa: an association with ciliary abnormalitiesPMID 1733835Read ↗

RPGR: part one of the X-linked retinitis pigmentosa story.Semantic proximity Read ↗

Insights into X-linked retinitis pigmentosa type 3, allied diseases and underlying pathomechanisms.Semantic proximity Read ↗

Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. Online.Semantic proximity Read ↗

A novel locus for X-linked retinitis pigmentosa.Semantic proximity Read ↗

Novel RPGR mutations with distinct retinitis pigmentosa phenotypes in French-Canadian families.Semantic proximity Read ↗

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

Novel mutations of the RPGR gene in RP3 families.Semantic proximity Read ↗

A novel locus (RP33) for autosomal dominant retinitis pigmentosa mapping to chromosomal region 2cen-q12.1Semantic proximity Read ↗

Five novel RPGR mutations in families with X-linked retinitis pigmentosa.Semantic proximity Read ↗

Novel variants of RPGR in X-linked retinitis pigmentosa families and genotype-phenotype correlation.Semantic proximity Read ↗

RPGR and RP2: targets for the treatment of X-linked retinitis pigmentosa?Semantic proximity Read ↗

Mutations of RPGR in X-linked retinitis pigmentosa (RP3).Semantic proximity Read ↗

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