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Article

Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?

Neurology - 20 Nov 2007

Charles P, Camuzat A, Benammar N, Sellal F, Destée A, Bonnet A-M, Lesage S, Le Ber I, Stevanin G, Dürr A, Brice A

Abstract excerpt

BACKGROUND: Autosomal dominant parkinsonism (ADP) is caused in a large percentage of familial and sporadic cases by mutations in the LRRK2 gene, particularly G2019S. It is also caused by mutations in genes associated with autosomal dominant cerebellar ataxia (ADCA), notably CAG/CAA repeat expansi...

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Identifiers

PMID: 17568014
DOI: 10.1212/01.wnl.0000269323.21969.db

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17568014-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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