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Article

Slow saccades and other eye movement disorders in spinocerebellar atrophy type 1.

Journal of neurology - 1 Feb 1997

Klostermann W, Zühlke C, Heide W, Kömpf D, Wessel K

Abstract excerpt

In order to study the relation between genotype and phenotype, a detailed study of the course of oculomotor deficits was performed in three patients with autosomal-dominant cerebellar ataxia, subtype spinocerebellar atrophy type 1 (SCA 1) using clinical testing and electrooculography. DNA analysis revealed a CAG repeat expansion of 65 in the SCA 1 gene on chromosome 6p in all patients. A progressive disorder of...

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Identifiers

PMID: 9120492
DOI: 10.1007/s004150050058

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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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