Add to ORKGBackgroundWomen who carry a premutation allele of the FMR1 gene are at increased vulnerability to an array of age-related symptoms and disorders, including age-related decline in select cognitive skills. However, the risk factors for age-related decline are poorly understood, including the potential role of family history and genetic factors. In other forms of pathological aging, early decline in syntactic complexity is observed and predicts the later onset of neurodegenerative disease. To shed light on the earliest signs of degeneration, the present study characterized longitudinal changes in the syntactic complexity of women with the FMR1 premutation across midlife, and associations with family history of fragile X-associated tremor/ataxi...
Fragile X syndrome (FXS) is one of three syndromes identified as a health condition related to fragi...
It is generally thought that fragile X-associated tremor/ataxia syndrome (FXTAS) represents a late-o...
BackgroundCarriers of the FMR1 premutation are at increased risk of developing a late-onset progress...
BackgroundWomen who carry a premutation allele of the FMR1 gene are at increased vulnerability to an...
BACKGROUND: Women who carry a premutation allele of the FMR1 gene are at increased vulnerability to ...
BACKGROUND: Male carriers of the FMR1 premutation are at risk of developing the fragile X-associated...
BACKGROUND: Smaller expansions of CGG trinucleotide repeats in the FMR1 X-linked gene termed 'premut...
Abstract Background Smaller expansions of CGG trinucleotide repeats in the FMR1 X-linked gene termed...
The 5′ untranslated region of the fragile X mental retardation gene, FMR1, contains a polymorphic CG...
The fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder c...
Fragile X premutation (FXPM) is a genetic mutation of the FMR1 gene characterized by having between ...
The CGG-repeat present in the 5'UTR of the FMR1 gene is unstable upon transmission to the next gener...
Fragile X Syndrome is a genetic disorder caused by a mutation on the X chromosome and is known to be...
Many studies have focused on the behavior and cognitive problems in young patients with fragile X sy...
Fragile X syndrome (FXS) is the most common single gene cause of intellectual disability and autism ...
Fragile X syndrome (FXS) is one of three syndromes identified as a health condition related to fragi...
It is generally thought that fragile X-associated tremor/ataxia syndrome (FXTAS) represents a late-o...
BackgroundCarriers of the FMR1 premutation are at increased risk of developing a late-onset progress...
BackgroundWomen who carry a premutation allele of the FMR1 gene are at increased vulnerability to an...
BACKGROUND: Women who carry a premutation allele of the FMR1 gene are at increased vulnerability to ...
BACKGROUND: Male carriers of the FMR1 premutation are at risk of developing the fragile X-associated...
BACKGROUND: Smaller expansions of CGG trinucleotide repeats in the FMR1 X-linked gene termed 'premut...
Abstract Background Smaller expansions of CGG trinucleotide repeats in the FMR1 X-linked gene termed...
The 5′ untranslated region of the fragile X mental retardation gene, FMR1, contains a polymorphic CG...
The fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder c...
Fragile X premutation (FXPM) is a genetic mutation of the FMR1 gene characterized by having between ...
The CGG-repeat present in the 5'UTR of the FMR1 gene is unstable upon transmission to the next gener...
Fragile X Syndrome is a genetic disorder caused by a mutation on the X chromosome and is known to be...
Many studies have focused on the behavior and cognitive problems in young patients with fragile X sy...
Fragile X syndrome (FXS) is the most common single gene cause of intellectual disability and autism ...
Fragile X syndrome (FXS) is one of three syndromes identified as a health condition related to fragi...
It is generally thought that fragile X-associated tremor/ataxia syndrome (FXTAS) represents a late-o...
BackgroundCarriers of the FMR1 premutation are at increased risk of developing a late-onset progress...