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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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Detalles Bibliográficos
Autores principales:	Ananbeh, Hanadi, Vodicka, Petr, Kupcova Skalnikova, Helena
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8071291/ https://www.ncbi.nlm.nih.gov/pubmed/33920936 http://dx.doi.org/10.3390/ijms22084085

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