Journal article
White matter changes in patients with parkinson's disease carrying small CGG expansion FMR1 alleles: A pilot study
N Trost, M Cook, E Hammersley, MQ Bui, P Brotchie, T Burgess, H Slater, E Storey, DZ Loesch
Neurodegenerative Diseases | Published : 2014
DOI: 10.1159/000356190
Abstract
Background/Aims: Alleles of the FMR1 gene containing small expansions of the CGG-trinucleotide repeat comprise premutation and grey-zone alleles. Premutation alleles may cause late-onset Fragile X-associated tremor/ataxia syndrome attributed to the neurotoxic effect of elevated FMR1 transcripts. Our earlier data suggested that both grey-zone and low-end premutation alleles might also play a significant role in the acquisition of the parkinsonian phenotype due to mitochondrial dysfunction caused by elevated FMR1 mRNA toxicity. These data were obtained through clinical and molecular comparisons between carriers of grey-zone/low-end premutation alleles and group-matched non-carrier controls fro..
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Awarded by National Institute of Child Health and Human Development
Funding Acknowledgements
This study was supported by the National Institutes of Child Health and Human Development Grant HD 36071, and NHMRC project grant No. 330400, to D.Z.L.