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Multiple system atrophy: genetic risks and alpha-synuclein mutations
Multiple system atrophy (MSA) is one of the few neurodegenerative disorders where we have a significant understanding of the clinical and pathological manifestations but where the aetiology remains almost completely unknown. Research to overcome this hurdle is gaining momentum through international...
Shranjeno v:
| izdano v: | F1000Res |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
F1000 Research Limited
2017
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5710304/ https://ncbi.nlm.nih.gov/pubmed/29225795 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.12193.1 |
| Oznake: |
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