Impaired cortico-striatal functional connectivity in prodromal Huntington’s Disease

Huntington’s Disease (HD) is a neurodegenerative disease caused by a CAG triplet-repeat expansion-mutation in the Huntingtin gene. Subjects at risk for HD can be identified by genetic testing in the prodromal phase. Structural changes of basal-ganglia nuclei such as the caudate nucleus are well-repl...

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Detalhes bibliográficos
Main Authors: Unschuld, Paul G., Joel, Suresh E., Liu, Xinyang, Shanahan, Megan, Margolis, Russell L., Biglan, Kevin M., Bassett, Susan S., Schretlen, David J., Redgrave, Graham W., van Zijl, Peter C.M., Pekar, James J., Ross, Christopher A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3331724/
https://ncbi.nlm.nih.gov/pubmed/22425717
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2012.02.095
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