## Abstract The cerebellar variant of multiple system atrophy (MSAβC) has overlapping clinical features with the hereditary spinocerebellar ataxias (SCAs), but can usually be distinguished on a clinical basis. We describe a patient who developed a sporadic, lateβonset, rapidly progressive neurodege
β¦ LIBER β¦
A Novel Frameshift Mutation in the AFG3L2 Gene in a Patient with Spinocerebellar Ataxia
β Scribed by Musova, Zuzana; Kaiserova, Michaela; Kriegova, Eva; Fillerova, Regina; Vasovcak, Peter; Santava, Alena; Mensikova, Katerina; Zumrova, Alena; Krepelova, Anna; Sedlacek, Zdenek; Kanovsky, Petr
- Book ID
- 121600208
- Publisher
- Springer-Verlag
- Year
- 2013
- Tongue
- English
- Weight
- 349 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1473-4222
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