Approximately 30–40% of male and 8–16% of female carriers of the Fragile X premutation will develop a neurodegenerative movement disorder characterized by intentional tremor, gait ataxia, autonomic dysfunction, cognitive decline, and Parkinsonism during their lifetime. At the molecular level, premutation carriers have increased expression levels of the FMR1 and the antisense FMR1 (ASFMR1) mRNAs. Both genes undergo alternative splicing giving rise to a number of different transcripts. Alteration in the alternative splicing process might be associated with FXTAS. In this study, we have investigated the correlation between objective measures of movement (balance and tremor using the CATSYS battery) and the expression of both the FMR1 and the A...
seng, E., Tang, H.-T., AlOlaby, R. R., Hickey, L. & Tassone, F. Altered expression of the FMR1 splic...
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a neurodegenerative disorder with defining cl...
BackgroundOver 40% of male and ∼16% of female carriers of a premutation FMR1 allele (55-200 CGG repe...
Approximately 30-40% of male and 8-16% of female carriers of the Fragile X premutation will develop ...
Abstract Fragile X associated tremor/ataxia syndrome (FXTAS) is a late adult-onset neurodegenerative...
Fragile X associated tremor/ataxia syndrome (FXTAS) is a late adult-onset neurodegenerative disorder...
FMR1 premutation carriers (55-200 CGG repeats) are at risk for developing Fragile X-associated Tremo...
Background: Individuals with premutation alleles of the FMR1 gene are at risk of developing fragile ...
BACKGROUND: Individuals with premutation alleles of the fragile X mental retardation 1 (FMR1) gene a...
Fragile X tremor ataxia syndrome (FXTAS) is a late-onset disorder manifesting in a proportion of FMR...
Fragile X tremor ataxia syndrome (FXTAS) is a late-onset disorder manifesting in a proportion of FMR...
FMR1 premutation carriers (55-200 CGG repeats) are at risk for developing Fragile X-associated Tremo...
This work is licensed under a Creative Commons Attribution 4.0 International License.Background Ind...
While an established protocol exists for diagnosing individ-uals with the fragile X-associated tremo...
BackgroundFragile X premutation carriers are at increased risk for fragile X-associated tremor ataxi...
seng, E., Tang, H.-T., AlOlaby, R. R., Hickey, L. & Tassone, F. Altered expression of the FMR1 splic...
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a neurodegenerative disorder with defining cl...
BackgroundOver 40% of male and ∼16% of female carriers of a premutation FMR1 allele (55-200 CGG repe...
Approximately 30-40% of male and 8-16% of female carriers of the Fragile X premutation will develop ...
Abstract Fragile X associated tremor/ataxia syndrome (FXTAS) is a late adult-onset neurodegenerative...
Fragile X associated tremor/ataxia syndrome (FXTAS) is a late adult-onset neurodegenerative disorder...
FMR1 premutation carriers (55-200 CGG repeats) are at risk for developing Fragile X-associated Tremo...
Background: Individuals with premutation alleles of the FMR1 gene are at risk of developing fragile ...
BACKGROUND: Individuals with premutation alleles of the fragile X mental retardation 1 (FMR1) gene a...
Fragile X tremor ataxia syndrome (FXTAS) is a late-onset disorder manifesting in a proportion of FMR...
Fragile X tremor ataxia syndrome (FXTAS) is a late-onset disorder manifesting in a proportion of FMR...
FMR1 premutation carriers (55-200 CGG repeats) are at risk for developing Fragile X-associated Tremo...
This work is licensed under a Creative Commons Attribution 4.0 International License.Background Ind...
While an established protocol exists for diagnosing individ-uals with the fragile X-associated tremo...
BackgroundFragile X premutation carriers are at increased risk for fragile X-associated tremor ataxi...
seng, E., Tang, H.-T., AlOlaby, R. R., Hickey, L. & Tassone, F. Altered expression of the FMR1 splic...
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a neurodegenerative disorder with defining cl...
BackgroundOver 40% of male and ∼16% of female carriers of a premutation FMR1 allele (55-200 CGG repe...