Focal dystonia as a presenting sign of spinocerebellar ataxia 17-Reference-Cited by-同舟云学术

Focal dystonia as a presenting sign of spinocerebellar ataxia 17

Published:2004-02 Issue:2 Volume:19 Page:217-220
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Hagenah Johann M.,Zühlke Christine,Hellenbroich Yorck,Heide Wolfgang,Klein Christine

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference18 articles.

1. A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?;Koide;Hum Mol Genet,1999

2. Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of hereditary ataxia;Zühlke;Eur J Hum Genet,2001

3. SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein;Nakamura;Hum Mol Genet,2001

4. CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia;Fujigasaki;Brain,2001

5. “Cryptic” repeating triplets of purine and pyrimidines (cRRY(i)) are frequent and polymorphic: analysis of coding cRRY(i) in the proopiomelanocortin (POMC) and TATA-binding protein (TBP) genes;Gostout;Am J Med Genet,1993

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