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Article

Ocular motility in genetically defined autosomal dominant cerebellar ataxia.

American journal of ophthalmology - 1 May 2002

Durig Jacques S, Jen Joanna C, Demer Joseph L

Abstract excerpt

PURPOSE: To describe ocular motility in patients having genetically characterized dominant cerebellar ataxia. DESIGN: Observational case series. METHOD: Nine ataxic adults having the following molecular genetic diagnoses underwent ophthalmic examination and ocular motility recordings: four with spinocerebellar ataxia type 6 (SCA-6), three with SCA-3, one with SCA-1, and one with episodic ataxia type 2 (EA-2)....

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Identifiers

PMID: 11992880
DOI: 10.1016/s0002-9394(02)01328-4

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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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