Fragile-X–Associated Tremor/Ataxia Syndrome (FXTAS) in Females with the FMR1 Premutation - Hagerman, R.J.; Leavitt, B.R.; Farzin, F.; Jacquemont, S.; Greco, C.M.; Brunberg, J.A.; Tassone, F.; Hessl, D.; Harris, S.W.; Zhang, L.; Jardini, T.; Gane, L.W.; et al. (American journal of human genetics, 2004)
Keywords: Adult; Age of Onset; Aged; Aged, 80 and over; Ataxia - genetics; Ataxia - pathology; Biological and medical sciences; Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...); Female; Fragile X Mental Retardation Protein; Fragile X Syndrome - genetics; Genotype; Heterozygote; Humans; Male; Medical genetics; Medical sciences; Middle Aged; Nerve Tissue Proteins - genetics; RNA-Binding Proteins; Tremor - genetics; Tremor - pathology; Trinucleotide Repeats - genetics; Chromosome fragility; Nervous system diseases; Tremor; Central nervous system disease; Ataxia; Female; Fragile X syndrome; Neurological disorder; Cerebral disorder; Involuntary movement