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Article

In vivo imaging of the photoreceptor mosaic of a rod monochromat.

Vision research - 1 Nov 2008

Carroll Joseph, Choi Stacey S, Williams David R

Abstract excerpt

Complete achromatopsia (i.e., rod monochromacy) is a congenital vision disorder in which cone function is absent or severely diminished, often due to mutations in one of two components of the cone phototransduction cascade (transducin or the cyclic-nucleotide gated channel). Previous histological data concerning cone structure are conflicting; suggesting anywhere from normal numbers of foveal cones to a complete...

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Source

Open in PubMed Open full text

Identifiers

PMID: 18499214
DOI: 10.1016/j.visres.2008.04.006
PMCID: PMC2582057

Genes

CNGB3

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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