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Article

FMR1 gray-zone alleles: association with Parkinson's disease in women?

Movement disorders : official journal of the Movement Disorder Society - 15 Aug 2011

Hall Deborah A, Berry-Kravis Elizabeth, Zhang Wenting, Tassone Flora, Spector Elaine, Zerbe Gary, Hagerman Paul J, Ouyang Bichun, Leehey Maureen A

Abstract excerpt

Carriers of fragile X mental retardation 1 repeat expansions in the premutation range (55-200 CGG repeats), especially males, often develop tremor, ataxia, and parkinsonism. These neurological signs are believed to be a result of elevated levels of expanded CGG-repeat fragile X mental retardation 1 mRNA. The purpose of this study was to determine the prevalence of fragile X mental retardation 1 repeat expansions...

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Source

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Identifiers

PMID: 21567456
DOI: 10.1002/mds.23755
PMCID: PMC3934001

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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FMR1 gray-zone alleles: association with Parkinson's disease in women?PMID 21567456Read ↗

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Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism.Semantic proximity Read ↗

Parkinsonism, FXTAS, and FMR1 premutations.Semantic proximity Read ↗

Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism.Semantic proximity Read ↗

Screen for excess FMR1 premutation alleles among males with parkinsonism.Semantic proximity Read ↗

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