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Article

Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2).

Ophthalmic genetics - 1 Sept 1999

Rosenberg T, Schwahn U, Feil S, Berger W

Abstract excerpt

PURPOSE: To identify possible correlations between the putative mutations and the clinical characteristics in X-linked retinitis pigmentosa, RP2. DESIGN: A retrospective, descriptive clinical study. MATERIAL: The ophthalmological files on affected persons from three Danish families with identified pathogenic mutations in the RP2 gene. RESULTS: Mutation analysis in 14 Danish families with X-linked retinitis...

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Source

Identifiers

PMID: 10520237
DOI: 10.1076/opge.20.3.161.2278

Genes

RPGR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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