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Article

Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15.

American journal of ophthalmology - 1 Feb 2005

Demirci F Yesim K, Gupta Nisha, Radak Amy L, Rigatti Brian W, Mah Tammy S, Milam Ann H, Gorin Michael B

Abstract excerpt

PURPOSE: To evaluate the donor retina of a patient with X-linked cone-rod dystrophy caused by an RPGR exon ORF15 mutation. DESIGN: Histopathologic study of the retina. METHODS: The eye of a 69-year-old man was fixed at 1.6 hours postmortem and processed for histopathology and immunocytochemistry....

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Share to Atrophy
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15734019
DOI: 10.1016/j.ajo.2004.08.041

Genes

RPGR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-15734019-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

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Research trail→

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Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15.PMID 15734019Read ↗

Retinal histopathology of an XLRP carrier with a mutation in the RPGR exon ORF15.Semantic proximity Read ↗

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Mutations in the RPGR gene cause X-linked cone dystrophy.Semantic proximity Read ↗

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Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes.Semantic proximity Read ↗

Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15.Semantic proximity Read ↗

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X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15.Semantic proximity Read ↗

Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15.Semantic proximity Read ↗

Defining a Novel RPGR Phenotype of Sector Retinitis Pigmentosa With Cone Dystrophy.Semantic proximity Read ↗

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