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Article

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

12 Apr 2006

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 16612614
DOI: 10.1007/s00439-006-0168-3

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Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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A novel locus (RP33) for autosomal dominant retinitis pigmentosa mapping to chromosomal region 2cen-q12.1PMID 16612614Read ↗

Evidence for a novel autosomal dominant retinitis pigmentosa linked to chromosome 1p22.1-q12 in a Chinese family.Semantic proximity Read ↗

Mutations in known genes account for 58% of autosomal dominant retinitis pigmentosa (adRP).Semantic proximity Read ↗

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Confirmation of linkage and refinement of the RP28 locus for autosomal recessive retinitis pigmentosa on chromosome 2p14-p15 in an Indian family.Semantic proximity Read ↗

Molecular genetics of retinitis pigmentosaSemantic proximity Read ↗

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

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

Autosomal Dominant Retinitis Pigmentosa.Semantic proximity Read ↗

Autosomal dominant retinitis pigmentosa: a new multi-allelic marker (D3S621) genetically linked to the disease locus (RP4).Semantic proximity Read ↗

Identification of a Novel Gene on 10q22.1 Causing Autosomal Dominant Retinitis Pigmentosa (adRP).Semantic proximity Read ↗

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

Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerationsSemantic proximity Read ↗

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