Атаксия: литература


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Orr HT et al: Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet 4:221, 1993

Ouahchi К et al: Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein. Nat Genet 9:141, 1995

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Rosenberg RN: Spinocerebellar ataxias and ataxins. N Engl J Med 333:1351, 1995

Rosenberg RN: The genetic basis of ataxia. ClinNeurosci3:l, 1995

Rosenberg RN, Iannaccone ST: The prevention of neurogenetic disease. Arch Neurol 52:356, 1995

Servadio A et al: Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals. Nat Genet 10:94, 1995

Terry JB, Rosenberg RN: Frontal lobe ataxia. Surg Neurol 44:583, 1995

Zhuchenko О et al: Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alfa1A-voltage-dependent calcium channel. Nat Genet 15:62, 1997

Zoghbi H: Spinocerebellar ataxia and other disorders of trinucleotide repeats, in Textbook of Molecular Medicine, JL Jameson (ed.). Cambridge, MA, Blackwell Science, 1997

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