FRAXE intermediate alleles are associated with Parkinson’s disease
- 16 September 2004
- journal article
- research article
- Published by Elsevier in Neuroscience Letters
- Vol. 368 (1) , 21-24
- https://doi.org/10.1016/j.neulet.2004.06.049
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Gene Structure and Subcellular Localization of FMR2, a Member of a New Family of Putative Transcription ActivatorsGenomics, 1997
- FMR2 Expression in Families with Fraxe Mental RetardationHuman Molecular Genetics, 1997
- The Role of Size, Sequence and Haplotype in the Stability of FRAXA and FRAXE Alleles during TransmissionHuman Molecular Genetics, 1997
- Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothersHuman Molecular Genetics, 1996
- Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG islandNature Genetics, 1996
- Identification of the gene FMR2, associated with FRAXE mental retardationNature Genetics, 1996
- Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardationCell, 1993
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991
- The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease.Journal of Neurology, Neurosurgery & Psychiatry, 1988