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New susceptible variant of COQ2 gene in Japanese patients with sporadic multiple system atrophy

OBJECTIVE: The aim of this study was to analyze the association between the variations of coenzyme Q2 4-hydroxybenzoate polyprenyltransferase gene (COQ2) and Japanese patients with multiple system atrophy (MSA). METHODS: We investigated the genetic variations in exons 1, 2, 6, and 7 of the COQ2 gene...

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Detalles Bibliográficos
Publicado en:Neurol Genet
Main Authors: Sun, Zhuoran, Ohta, Yasuyuki, Yamashita, Toru, Sato, Kota, Takemoto, Mami, Hishikawa, Nozomi, Abe, Koji
Formato: Artigo
Idioma:Inglês
Publicado: Wolters Kluwer 2016
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4830192/
https://ncbi.nlm.nih.gov/pubmed/27123473
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000054
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