rCGG repeats in premutant alleles of the fragile X gene (FMR1) cause neurodegeneration in Drosophila and are thought to cause fragile X-associated tremor/ataxia syndrome in humans. Two reports in this issue of Neuron (Jin et al. and Sofola et al.) present data indicating a disease mechanism involving disruption of RNA-binding protein function
AbstractFragile X syndrome carriers have FMR1 alleles, called premutations, with an intermediate num...
SummaryFragile X-associated tremor/ataxia syndrome (FXTAS) is a recently described neurodegenerative...
Fragile X-associated Tremor/Ataxia Syndrome (FXTAS) is a progressive neurodegenerative disorder that...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an inherited neurodegen...
The CGG-repeat present in the 5'UTR of the FMR1 gene is unstable upon transmission to the next gener...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an inherited neurodegen...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an inherited neurodegen...
Fragile X syndrome, the most common heritable form of cognitive impairment, is caused by epigenetic ...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an adult-onset inherite...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an adult-onset inherite...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an adult-onset inherite...
Fragile X-associated tremor/ataxia syndrome (FXTAS) is an adult-onset inherited neurodegenerative di...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an adult-onset inherite...
Fragile X Syndrome is the most common form of hereditary mental retardation. It is caused by a large...
Jin et al. have clearly demonstrated that rCGG repeats can induce pathogenesis and mediate neurodege...
AbstractFragile X syndrome carriers have FMR1 alleles, called premutations, with an intermediate num...
SummaryFragile X-associated tremor/ataxia syndrome (FXTAS) is a recently described neurodegenerative...
Fragile X-associated Tremor/Ataxia Syndrome (FXTAS) is a progressive neurodegenerative disorder that...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an inherited neurodegen...
The CGG-repeat present in the 5'UTR of the FMR1 gene is unstable upon transmission to the next gener...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an inherited neurodegen...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an inherited neurodegen...
Fragile X syndrome, the most common heritable form of cognitive impairment, is caused by epigenetic ...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an adult-onset inherite...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an adult-onset inherite...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an adult-onset inherite...
Fragile X-associated tremor/ataxia syndrome (FXTAS) is an adult-onset inherited neurodegenerative di...
International audienceFragile X-associated tremor/ataxia syndrome (FXTAS) is an adult-onset inherite...
Fragile X Syndrome is the most common form of hereditary mental retardation. It is caused by a large...
Jin et al. have clearly demonstrated that rCGG repeats can induce pathogenesis and mediate neurodege...
AbstractFragile X syndrome carriers have FMR1 alleles, called premutations, with an intermediate num...
SummaryFragile X-associated tremor/ataxia syndrome (FXTAS) is a recently described neurodegenerative...
Fragile X-associated Tremor/Ataxia Syndrome (FXTAS) is a progressive neurodegenerative disorder that...
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