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See Latest ArticlesSpinocerebellar ataxia type 11 in the Chinese Han population
Neurological Sciences, 10/07/09
Xu Q et al. – To investigate the frequency of SCA11 in Chinese SCA patients, the authors examined the TTBK2 gene in 68 unrelated probands diagnosed with dominantly inherited ataxia using the denaturing high–performance liquid chromatography method. All analyzed samples displayed the normal elution profile, which denoted that no disease–related mutation was identified. They provided the evidence that SCA11 is a rare form of ataxia in China.
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