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Emerging Roles of Exosomes in Huntington’s Disease

Huntington’s disease (HD) is a rare hereditary autosomal dominant neurodegenerative disorder, which is caused by expression of mutant huntingtin protein (mHTT) with an abnormal number of glutamine repeats in its N terminus, and characterized by intracellular mHTT aggregates (inclusions) in the brain...

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Detalhes bibliográficos
Publicado no:Int J Mol Sci
Main Authors: Ananbeh, Hanadi, Vodicka, Petr, Kupcova Skalnikova, Helena
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8071291/
https://ncbi.nlm.nih.gov/pubmed/33920936
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22084085
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