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Mutation Analysis of COQ2 in Chinese Patients with Cerebellar Subtype of Multiple System Atrophy
AIMS: Recently, mutations in COQ2 encoding para‐hydroxybenzoate‐polyprenyl transferase have been identified to increase the risk of multiple system atrophy (MSA) in multiplex families and sporadic cases. The prevalence of COQ2 mutations was showed to be higher in cerebellar subtype (MSA‐C) than park...
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| Publicado no: | CNS Neurosci Ther |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6495228/ https://ncbi.nlm.nih.gov/pubmed/26096180 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cns.12412 |
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