(redirected from Autosomal Dominant Cerebellar Ataxia)
AADCAAutosomal Dominant Cerebellar Ataxia (disease)
Copyright 1988-2018 AcronymFinder.com, All rights reserved.
References in periodicals archive ?
The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1.
Clinical and molecular advances in autosomal dominant cerebellar ataxias: From genotype to phenotype and physiopathology.
Autosomal dominant cerebellar ataxias: Polyglutamine expansions and beyond.
(1997) Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.
(1) The prevalence of the autosomal dominant cerebellar ataxias is reported to be 1-5:100,000 population.
Riess, "Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis," The Lancet Neurology, vol.
Full browser ?