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Huntington's disease: Molecular basis of pathology and status of current therapeutic approaches
Huntington's disease (HD) is a frequent and incurable hereditary neurodegenerative disorder that impairs motor and cognitive functions. Mutations in huntingtin (HTT) protein, which is essential for neuronal development, lead to the development of HD. An increase in the number of CAG repeats wit...
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| Publicat a: | Exp Ther Med |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
D.A. Spandidos
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5038571/ https://ncbi.nlm.nih.gov/pubmed/27698679 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2016.3566 |
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