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In vivo molecular signatures of cerebellar pathology in spinocerebellar ataxia type 3
BACKGROUND: No treatment exists for the most common dominantly inherited ataxia Machado-Joseph disease, or spinocerebellar ataxia type 3 (SCA3). Successful evaluation of candidate therapeutics will be facilitated by validated noninvasive biomarkers of disease pathology recapitulated by animal models...
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| Vydáno v: | Mov Disord |
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| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7572607/ https://ncbi.nlm.nih.gov/pubmed/32621646 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.28140 |
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