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Article

Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations.

Investigative ophthalmology & visual science - 1 Oct 2007

Aleman Tomas S, Cideciyan Artur V, Sumaroka Alexander, Schwartz Sharon B, Roman Alejandro J, Windsor Elizabeth A M, Steinberg Janet D, Branham Kari, Othman Mohammad, Swaroop Anand, Jacobson Samuel G

Abstract excerpt

PURPOSE: To investigate in vivo the retinal microstructure in X-linked retinitis pigmentosa (XLRP) caused by RPGR mutations as a prelude to treatment initiatives for this common form of RP. METHODS: Patients with RPGR-XLRP (n = 12; age range, 10-56 years) were studied by optical coherence tomogra...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 17898302
DOI: 10.1167/iovs.07-0453
PMCID: PMC3178894

Genes

RPGR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17898302-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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