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Striatal GABAergic interneuron dysfunction in the Q175 mouse model of Huntington’s disease

The pathological hallmark of Huntington’s disease (HD) is the massive loss of striatal and cortical neurons. Until recently, it was believed that striatal interneurons were spared from degeneration. This view has changed after the demonstration that parvalbumin (PV)-expressing interneurons also are...

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Bibliografske podrobnosti
izdano v:Eur J Neurosci
Main Authors: Holley, Sandra M., Galvan, Laurie, Kamdjou, Talia, Cepeda, Carlos, Levine, Michael S.
Format: Artigo
Jezik:Inglês
Izdano: 2018
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC8320683/
https://ncbi.nlm.nih.gov/pubmed/30472747
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ejn.14283
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