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Article

New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease.

Clinical genetics - 1 Oct 2013

Loesch D Z, Tassone F, Lo J, Slater H R, Hills L V, Bui M Q, Silburn P A, Mellick G D

Abstract excerpt

We recently reported a significant increase in the frequency of carriers of grey zone (GZ) alleles of FMR1 gene in Australian males with Parkinson's disease (PD) from Victoria and Tasmania. Here, we report data comparing an independent sample of 817 PD patients from Queensland to 1078 consecutive Australian male newborns from Victoria. We confirmed the earlier finding by observing a significant excess of GZ...

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Source

Identifiers

PMID: 23198693
DOI: 10.1111/cge.12070

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease.PMID 23198693Read ↗

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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 ↗

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