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Molecular Targets and Therapeutic Strategies in Spinocerebellar Ataxia Type 7
Spinocerebellar ataxia type 7 (SCA7) is a rare autosomal dominant neurodegenerative disorder characterized by progressive neuronal loss in the cerebellum, brainstem, and retina, leading to cerebellar ataxia and blindness as major symptoms. SCA7 is due to the expansion of a CAG triplet repeat that is...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Neurotherapeutics |
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| Κύριοι συγγραφείς: | , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Springer International Publishing
2019
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6985300/ https://ncbi.nlm.nih.gov/pubmed/31432449 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13311-019-00778-5 |
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