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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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Front Neurol
Prif Awduron: Wilson, Heather, De Micco, Rosa, Niccolini, Flavia, Politis, Marios
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Frontiers Media S.A. 2017
Pynciau:
Mynediad Ar-lein: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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