Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10745063 | Parkinsonism & Related Disorders | 2015 | 4 Pages |
Abstract
SCA12 might not be as rare in Chinese as previously assumed. The identification of the shortest pathogenic allele helps to define the minimal limit implicated in the disease onset. Moreover, the disease manifestations distinct from other SCA subtypes could help clinicians to provide timely genetic counseling.
Keywords
Related Topics
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Biochemistry, Genetics and Molecular Biology
Ageing
Authors
Yi Dong, Jian-Jun Wu, Zhi-Ying Wu,