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Article

Parkinsonism, FXTAS, and FMR1 premutations.

Movement disorders : official journal of the Movement Disorder Society - 1 Feb 2005

Toft Mathias, Aasly Jan, Bisceglio Gina, Adler Charles H, Uitti Ryan J, Krygowska-Wajs Anna, Lynch Timothy, Wszolek Zbigniew K, Farrer Matthew J

Abstract excerpt

The presence of late-onset neurological symptoms in male carriers of premutation expansions of the fragile X mental retardation 1 (FMR1) gene has been described recently. One of the clinical symptoms in this fragile X-associated tremor/ataxia syndrome (FXTAS) is parkinsonism. To test the possible association between expanded FMR1 alleles and Parkinson's disease (PD), we determined the size of the FMR1 CGG repeat...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15390127
DOI: 10.1002/mds.20297

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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