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Article

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

1 Feb 2003

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 12634863
DOI: 10.1038/sj.ejhg.5200942

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Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerationsPMID 12634863Read ↗

Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene.Semantic proximity Read ↗

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RP1 and autosomal dominant rod-cone dystrophy: novel mutations, a review of published variants, and genotype-phenotype correlation.Semantic proximity Read ↗

Toward an elucidation of the molecular genetics of inherited retinal degenerations.Semantic proximity Read ↗

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Retinitis pigmentosa and allied conditions today: a paradigm of translational researchSemantic proximity Read ↗

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