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Article

Fragile X gene premutation in multiple system atrophy.

Journal of the neurological sciences - 15 Dec 2004

Garland E M, Vnencak-Jones C L, Biaggioni I, Davis T L, Montine T J, Robertson D

Abstract excerpt

Previous reports have suggested that expansion of the CGG repeat located in the fragile X mental retardation 1 (FMR1) gene might be responsible for a significant number of patients with the multiple system atrophy (MSA) phenotype. Analysis of 65 MSA patients found only 4.6% displayed CGG expansions in the suspected range. This is similar to the frequency reported in the normal population, suggesting that this...

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Source

Identifiers

PMID: 15546601
DOI: 10.1016/j.jns.2004.08.013

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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