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Characterization of axonal transport defects in Drosophila Huntingtin mutants
Polyglutamine (polyQ) expansion within Huntingtin (Htt) causes the fatal neurodegenerative disorder Huntington’s Disease (HD). Although Htt is ubiquitously expressed and conserved from Drosophila to humans, its normal biological function is still being elucidated. Here we characterize a role for the...
Gardado en:
| Publicado en: | J Neurogenet |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2016
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5525331/ https://ncbi.nlm.nih.gov/pubmed/27309588 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/01677063.2016.1202950 |
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