## Abstract The fragile X‐associated tremor/ataxia syndrome (FXTAS) is a recently identified phenotype associated with trinucleotide repeat expansions in the premutation range of the fragile X mental retardation 1 (__FMR1__) gene. In addition to progressive gait ataxia, action tremor, peripheral ne
✦ LIBER ✦
Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS)
✍ Scribed by Jim Grigsby; Angela G. Brega; Sébastien Jacquemont; Danuta Z. Loesch; Maureen A. Leehey; Glenn K. Goodrich; Randi J. Hagerman; Jennifer Epstein; Rebecca Wilson; Jennifer B. Cogswell; Tristan Jardini; Flora Tassone; Paul J. Hagerman
- Book ID
- 119301986
- Publisher
- Elsevier Science
- Year
- 2006
- Tongue
- English
- Weight
- 116 KB
- Volume
- 248
- Category
- Article
- ISSN
- 0022-510X
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## Abstract ## Background Fragile X‐associated tremor/ataxia syndrome (FXTAS), which occurs in some premutation carriers of the fragile X mental retardation 1 (__FMR1__) gene, is a neurodegenerative disorder characterized by action tremor, gait ataxia, and impaired executive cognitive functioning.
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