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Article

Autosomal dominant inheritance of a negative electroretinogram phenotype in three generations.

American journal of ophthalmology - 1 Apr 2001

Fitzgerald K M, Hashimoto T, Hug T E, Cibis G W, Harris D J

Abstract excerpt

PURPOSE: We report an abnormal electroretinogram with a negative configuration in a child who presented with moderate myopia, nystagmus, and visual developmental delay. We investigated the electroretinogram and explored the possibility of a metabotropic glutamate receptor subtype 6 mutation in six family members spanning four generations. METHODS: Case report and family study: Complete eye examinations and...

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Source

Identifiers

PMID: 11292414
DOI: 10.1016/s0002-9394(00)00849-7

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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