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Spinocerebellar ataxia 35

25 Sept 2014

Abstract excerpt

OBJECTIVE: To elucidate the clinical and cellular characteristics of spinocerebellar ataxia type 35 (SCA35), which is caused by mutations in the TGM6 gene encoding transglutaminase 6 (TG6), in a Taiwanese cohort. METHODS: Mutations in TGM6 were ascertained in 109 unrelated probands of Chinese descent with molecularly unassigned SCA from 512 pedigrees, in whom mutations responsible for 15 other ataxia syndromes...

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PMID: 25253745
DOI: 10.1212/wnl.0000000000000909

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