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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...
שמור ב:
| הוצא לאור ב: | CNS Neurosci Ther |
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| Main Authors: | , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
John Wiley and Sons Inc.
2015
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| נושאים: | |
| גישה מקוונת: | 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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