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Pathogenic mechanisms underlying spinocerebellar ataxia type 1
The family of hereditary cerebellar ataxias is a large group of disorders with heterogenous clinical manifestations and genetic etiologies. Among these, over 30 autosomal dominantly inherited subtypes have been identified, collectively referred to as the spinocerebellar ataxias (SCAs). Generally, th...
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| Publicado no: | Cell Mol Life Sci |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer International Publishing
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7541529/ https://ncbi.nlm.nih.gov/pubmed/32306062 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00018-020-03520-z |
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