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Article

Autosomal dominant cerebellar ataxia type I. Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3.

Brain : a journal of neurology - 1 Dec 1997

Abele M, Bürk K, Andres F, Topka H, Laccone F, Bösch S, Brice A, Cancel G, Dichgans J, Klockgether T

Abstract excerpt

Forty-one patients suffering from autosomal dominant cerebellar ataxia type I (ADCA-I) were subjected to a genotype-phenotype correlation analysis using molecular genetic assignment to the spinocerebellar ataxia type 1, 2 or 3 (SCA1, -2 or -3) genetic locus, clinical examination and nerve conduct...

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Source

Identifiers

PMID: 9448569
DOI: 10.1093/brain/120.12.2141

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-9448569-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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