COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese

Mov Disord. 2015 Mar;30(3):436-7. doi: 10.1002/mds.26138. Epub 2015 Jan 16.

Authors

Chin-Hsien Lin¹, Eng-King Tan, Chih-Chao Yang, Zhao Yi, Ruey-Meei Wu

Affiliation

¹ Department of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan.

PMID: 25594503
DOI: 10.1002/mds.26138

No abstract available

Keywords: COQ2; Parkinson's disease: coenzyme Q10; mitochondria; multiple system atrophy.

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Alkyl and Aryl Transferases / genetics*
Asian People / genetics
Cerebellum / pathology*
Female
Gene Frequency
Genotype
Humans
Male
Multiple System Atrophy / genetics*
Multiple System Atrophy / pathology*
Odds Ratio
Polymorphism, Single Nucleotide / genetics*

Substances

Alkyl and Aryl Transferases
4-hydroxybenzoate polyprenyltransferase