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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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| Publicat a: | Cell Mol Life Sci |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer International Publishing
2020
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| Matèries: | |
| Accés en línia: | 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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