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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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Bibliografski detalji
Izdano u:Front Neurol
Glavni autori: Wilson, Heather, De Micco, Rosa, Niccolini, Flavia, Politis, Marios
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2017
Teme:
Online pristup: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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