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Possible involvement of self-defense mechanisms in the preferential vulnerability of the striatum in Huntington's disease

HD is caused by a mutation in the huntingtin gene that consists in a CAG repeat expansion translated into an abnormal poly-glutamine (polyQ) tract in the huntingtin (Htt) protein. The most striking neuropathological finding in HD is the atrophy of the striatum. The regional expression of mutant Htt...

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Detaylı Bibliyografya
Asıl Yazarlar: Francelle, Laetitia, Galvan, Laurie, Brouillet, Emmanuel
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2014
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4176035/
https://ncbi.nlm.nih.gov/pubmed/25309327
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2014.00295
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