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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 en: | Cell Mol Life Sci |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Springer International Publishing
2020
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| Assuntos: | |
| Acceso en liña: | 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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