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Molecular Mechanisms and Future Therapeutics for Spinocerebellar Ataxia Type 31 (SCA31)
Spinocerebellar ataxia type 31 (SCA31) is one of the autosomal-dominant neurodegenerative disorders that shows progressive cerebellar ataxia as a cardinal symptom. This disease is caused by a 2.5- to 3.8-kb-long complex pentanucleotide repeat containing (TGGAA)(n), (TAGAA)(n), (TAAAA)(n), and (TAAAA...
Tallennettuna:
| Julkaisussa: | Neurotherapeutics |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Springer International Publishing
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6985187/ https://ncbi.nlm.nih.gov/pubmed/31755042 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13311-019-00804-6 |
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