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Article

High-resolution optical coherence tomography imaging in KCNV2 retinopathy.

The British journal of ophthalmology - 1 Feb 2012

Sergouniotis Panagiotis I, Holder Graham E, Robson Anthony G, Michaelides Michel, Webster Andrew R, Moore Anthony T

Abstract excerpt

AIM: To report novel spectral domain optical coherence tomography (SD-OCT) findings and new mutational data in patients with 'cone dystrophy with supernormal rod electroretinogram', a recessive childhood onset retinal dystrophy consequent upon mutation in the KCNV2 gene. DESIGN/METHODS: This was a comparative case series study of 12 patients with clinical and/or electrophysiological findings in keeping with KCNV2...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 21558291
DOI: 10.1136/bjo.2011.203638

Genes

KCNV2
RPE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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