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Multiple system atrophy: the application of genetics in understanding etiology
Classically defined phenotypically by a triad of cerebellar ataxia, parkinsonism and autonomic dysfunction in conjunction with pyramidal signs, multiple system atrophy (MSA) is a rare and progressive neurodegenerative disease affecting an estimated 3-4 per every 100,000 individuals among adults 50-9...
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| Publicado no: | Clin Auton Res |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5217460/ https://ncbi.nlm.nih.gov/pubmed/25687905 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10286-014-0267-5 |
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