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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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Détails bibliographiques
Publié dans:Front Neurol
Auteurs principaux: Wilson, Heather, De Micco, Rosa, Niccolini, Flavia, Politis, Marios
Format: Artigo
Langue:Inglês
Publié: Frontiers Media S.A. 2017
Sujets:
Accès en ligne: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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