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Article

Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations.

Investigative ophthalmology & visual science - 1 Apr 2008

Aleman Tomas S, Cideciyan Artur V, Sumaroka Alexander, Windsor Elizabeth A M, Herrera Waldo, White D Alan, Kaushal Shalesh, Naidu Anjani, Roman Alejandro J, Schwartz Sharon B, Stone Edwin M, Jacobson Samuel G

Abstract excerpt

PURPOSE: To determine the underlying retinal micropathology in subclasses of autosomal dominant retinitis pigmentosa (ADRP) caused by rhodopsin (RHO) mutations. METHODS: Patients with RHO-ADRP (n = 17, ages 6-73 years), representing class A (R135W and P347L) and class B (P23H, T58R, and G106R) functional phenotypes, were studied with optical coherence tomography (OCT), and colocalized visual thresholds were...

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Identifiers

PMID: 18385078
DOI: 10.1167/iovs.07-1110
PMCID: PMC3179264

Genes

RHO
RPE

Variants

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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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