Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1916448 | Journal of the Neurological Sciences | 2007 | 4 Pages |
Abstract
The mtDNA mutations A3243G, A8344G, T8993G, T8993C, or POLG1 W748S and A467T are very rare causes of adult-onset ataxia in Taiwan. Routine screening for these mutations in ataxia patients with Chinese origin is of limited clinical value.
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Authors
Yi-Chung Lee, Yi-Chun Lu, Ming-Hon Chang, Bing-Wen Soong,