Autosomal dominant cerebellar ataxias are a heterogeneous group of neurodegenerative disorders that generally present in adulthood. Spinocerebellar ataxia type 2 typically presents with progressive cerebellar symptoms, slow ocular saccades, and peripheral neuropathy. The onset of symptoms is usually
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Spinocerebellar ataxia type 2 (SCA2) in an Egyptian family presenting with polyphagia and marked CAG expansion in infancy
โ Scribed by A. Abdel-Aleem; M. S. Zaki
- Publisher
- Springer
- Year
- 2008
- Tongue
- English
- Weight
- 427 KB
- Volume
- 255
- Category
- Article
- ISSN
- 0340-5354
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