Genetics Modulate Gray Matter Variation Beyond Disease Burden in Prodromal Huntington’s Disease

Huntington’s disease (HD) is a neurodegenerative disorder caused by an expansion mutation of the cytosine–adenine–guanine (CAG) trinucleotide in the HTT gene. Decline in cognitive and motor functioning during the prodromal phase has been reported, and understanding genetic influences on prodromal di...

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Detalhes bibliográficos
Publicado no:Front Neurol
Main Authors: Liu, Jingyu, Ciarochi, Jennifer, Calhoun, Vince D., Paulsen, Jane S., Bockholt, H. Jeremy, Johnson, Hans J., Long, Jeffrey D., Lin, Dongdong, Espinoza, Flor A., Misiura, Maria B., Caprihan, Arvind, Turner, Jessica A.
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2018
Assuntos:
Neuroscience
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5884935/
https://ncbi.nlm.nih.gov/pubmed/29651271
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2018.00190
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