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Article

COQ2 variants in Parkinson's disease and multiple system atrophy.

Journal of neural transmission (Vienna, Austria : 1996) - 1 Jun 2018

Mikasa Michitaka, Kanai Kazuaki, Li Yuanzhe, Yoshino Hiroyo, Mogushi Kaoru, Hayashida Arisa, Ikeda Aya, Kawajiri Sumihiro, Okuma Yasuyuki, Kashihara Kenichi, Sato Tatsuya, Kondo Hiroshi, Funayama Manabu, Nishioka Kenya, Hattori Nobutaka

Abstract excerpt

Coenzyme Q2, polyprenyltransferase (COQ2) variants have been reported to be associated with multiple system atrophy (MSA). However, the relationship between COQ2 variants and familial Parkinson's disease (PD) remains unclear. We investigated the frequency of COQ2 variants and clinical symptoms among familial PD and MSA. We screened COQ2 using the Sanger method in 123 patients with familial PD, 52 patients with...

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Source

Identifiers

PMID: 29644397
DOI: 10.1007/s00702-018-1885-1

Genes

COQ2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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