Clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypes
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference36 articles.
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2. Clinical and genetic aspects of spinocerebellar degeneration
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4. Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia
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