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New alternative splicing variants of the ATXN2 transcript
BACKGROUND: Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant disorder with progressive degeneration of cerebellar Purkinje cells and selective loss of neurons in the brainstem. This neurodegenerative disorder is caused by the expansion of a polyglutamine domain in ataxin-2. Ataxin-2 is...
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| Publicado no: | Neurol Res Pract |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7650068/ https://ncbi.nlm.nih.gov/pubmed/33324888 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s42466-019-0025-1 |
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