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Article

SCA31 is rare in the Chinese population on Taiwan.

Neurobiology of aging - 1 Feb 2012

Lee Yi-Chung, Liu Chin-San, Lee Tzu-Ying, Lo Yang-Chung, Lu Yi-Chun, Soong Bing-Wen

Abstract excerpt

Spinocerebellar ataxia (SCA) is a clinically, pathologically, and genetically heterogeneous group of dominantly inherited neurodegenerative disorders. SCA31 has recently been reported to be associated with a complex penta-nucleotide (TGGAA)n repeat insertion in the introns of TK2 and BEAN. In this study we excluded SCA31 mutation from 119 unrelated patients with molecularly unassigned hereditary cerebellar...

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PMID: 21163552
DOI: 10.1016/j.neurobiolaging.2010.10.012

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