Article ID Journal Published Year Pages File Type
1916448 Journal of the Neurological Sciences 2007 4 Pages PDF
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.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Ageing
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