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Article

Common mitochondrial DNA and POLG1 mutations are rare in the Chinese patients with adult-onset ataxia on Taiwan.

Journal of the neurological sciences - 15 Mar 2007

Lee Yi-Chung, Lu Yi-Chun, Chang Ming-Hon, Soong Bing-Wen

Abstract excerpt

BACKGROUND AND PURPOSE: Spinocerebellar ataxia (SCA) is a heterogeneous group of neurodegenerative disorders with common features of adult-onset cerebellar ataxia. Many patients with clinically suspected SCA are subsequently diagnosed with common SCA gene mutations. Previous reports suggest some common mitochondrial DNA (mtDNA) point mutations and mitochondrial DNA polymerase gene (POLG1) mutations might be...

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Identifiers

PMID: 17300808
DOI: 10.1016/j.jns.2007.01.005

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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