Clinical and genetic analysis of spinocerebellar ataxia type 11
โ Scribed by Janel Johnson; Nicholas Wood; Paola Giunti; Henry Houlden
- Book ID
- 107648200
- Publisher
- Springer-Verlag
- Year
- 2008
- Tongue
- English
- Weight
- 226 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1473-4222
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## Abstract An increasing number of genetically defined types of spinocerebellar ataxia (SCA) have been reported in the past decade. Phenotypeโgenotype correlation studies have suggested a broad overlap between SCA types. The aim of the present study was to identify patterns of clinical features th
## Abstract The relative frequencies of different spinocerebellar ataxias (SCAs) vary widely among different ethnic groups, presumably due to a founder effect. We investigated the relative prevalence of SCA1โ3, 6โ8, 12, 17; dentateโrubroโpallidoluysian atrophy; and Friedreich's ataxia (FRDA) in Ser