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Article

Intrafamilial variability of Parkinson phenotype in SCAs: novel cases due to SCA2 and SCA3 expansions.

Parkinsonism & related disorders - 1 Jun 2009

Socal M P, Emmel V E, Rieder C R M, Hilbig A, Saraiva-Pereira M L, Jardim L B

Abstract excerpt

BACKGROUND: Parkinson's disease (PD) has been related to mutations associated with spinocerebellar ataxias (SCA); the frequency of the diagnosis of these mutations is low in general late-onset PD cases. Our aim was to investigate a selected high-risk group of PD patients. METHODS: PD patients wit...

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Identifiers

PMID: 18990604
DOI: 10.1016/j.parkreldis.2008.09.005

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-18990604-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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