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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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| Publicado no: | Exp Ther Med |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2016
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| Assuntos: | |
| Acesso em linha: | 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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