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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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| Pubblicato in: | Neurol Genet |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Wolters Kluwer
2016
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| Soggetti: | |
| Accesso online: | 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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