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Article

Foveal development and nystagmus.

Annals of the New York Academy of Sciences - 1 Sept 2011

Proudlock Frank, Gottlob Irene

Abstract excerpt

The combination of optical coherence tomography (OCT) and genetic methods along with other clinical diagnostic tools permit the discrimination of infantile nystagmus subtypes with a precision that has not previously been possible. Analysis of specific diseases, such as albinism and achromatopsia as well as known genetic abnormalities, such as FRMD7 and PAX6 mutations, shows subtle but significant differences...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Nystagmus, Congenital

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Source

Identifiers

PMID: 21951007
DOI: 10.1111/j.1749-6632.2011.06174.x

Genes

FRMD7
PAX6

Provenance

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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