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Article

Oligocone trichromacy is part of the spectrum of CNGA3-related cone system disorders.

Ophthalmic genetics - 1 Jun 2011

Vincent Ajoy, Wright Tom, Billingsley Gail, Westall Carol, Héon Elise

Abstract excerpt

PURPOSE: To report the rare observation of CNGA3 mutation as a cause of oligocone trichromacy (OT) and present phenotypic characteristics. METHODS: A 20 year old male patient underwent ophthalmological evaluation including detailed color vision assessment using Ishihara pseudoisochromatic plates, American Optical Hardy Rand Rittler plates (HRR) and Mollon-Reffin Minimalist test (MRM). Optical coherence tomography...

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Source

Identifiers

PMID: 21268679
DOI: 10.3109/13816810.2010.544366

Genes

CNGA3
CNGB3
ERG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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