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Molecular Imaging Markers to Track Huntington’s Disease Pathology

Huntington’s disease (HD) is a progressive, monogenic dominant neurodegenerative disorder caused by repeat expansion mutation in the huntingtin gene. The accumulation of mutant huntingtin protein, forming intranuclear inclusions, subsequently leads to degeneration of medium spiny neurons in the stri...

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Detalhes bibliográficos
Publicado no:Front Neurol
Main Authors: Wilson, Heather, De Micco, Rosa, Niccolini, Flavia, Politis, Marios
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5278260/
https://ncbi.nlm.nih.gov/pubmed/28194132
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2017.00011
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