Characterization of Neurodevelopmental Abnormalities in iPSC-Derived Striatal Cultures from Patients with Huntington’s Disease

BACKGROUND: Huntington’s disease (HD) is an inherited neurodegenerative disease and is characterized by atrophy of certain regions of the brain in a progressive manner. HD patients experience behavioral changes and uncontrolled movements which can be primarily attributed to the atrophy of striatal n...

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Detaylı Bibliyografya
Yayımlandı:J Huntingtons Dis
Asıl Yazarlar: Mathkar, Pranav P., Suresh, Divya, Dunn, James, Tom, Colton M., Mattis, Virginia B.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: IOS Press 2019
Konular:
Research Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6839479/
https://ncbi.nlm.nih.gov/pubmed/31381521
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JHD-180333
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