SCA8 should not be tested in isolation for ataxia
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Genetics(clinical),Clinical Neurology
Reference7 articles.
1. Recent advances in hereditary spinocerebellar ataxias;van de Warrenburg;J Neuropathol Exp Neurol,2005
2. SCA8 repeat expansions in ataxia: a controversial association;Sobrido;Neurology,2001
3. Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansion
4. Are (CTG)n expansions at the SCA8 locus rare polymorphisms?
5. Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia
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2. Genetic etiology of a Chinese ataxia cohort: Expanding the mutational spectrum of hereditary ataxias;Parkinsonism & Related Disorders;2021-08
3. The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins;Internal Medicine;2020-01-15
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