Title : Dysfunctional Dopaminergic Neurones in Mouse Models of Huntington's Disease: A Role for SK3 Channels.

Pub. Date : 2015

PMID : 25871323






1 Functional Relationships(s)
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1 BACKGROUND: Huntington"s disease (HD) is a late-onset fatal neurodegenerative disorder caused by a CAG trinucleotide repeat expansion in the gene coding for the protein huntingtin and is characterised by progressive motor, psychiatric and cognitive decline. trinucleotide huntingtin Mus musculus