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Article

A novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defect.

Visual neuroscience - 1 Jan 2000

Gunther Karen L, Neitz Jay, Neitz Maureen

Abstract excerpt

Inherited tritan color vision deficiency is caused by defects in the function of the short-wavelength-sensitive (S) cones. This heterozygous group of disorders has an autosomal dominant pattern of inheritance. Amino acid variations of the S cone opsin are rare and all that have been identified th...

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Identifiers

PMID: 16961973
DOI: 10.1017/S0952523806233169

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-16961973-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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A novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defect.PMID 16961973Read ↗

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