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The Phe932Ile mutation in KCNT1 channels associated with severe epilepsy, delayed myelination and leukoencephalopathy produces a loss-of-function channel phenotype

Sodium-activated potassium (K(Na)) channels contribute to firing frequency adaptation and slow afterhyperpolarization. The KCNT1 gene (also known as SLACK) encodes a K(Na) subunit that is expressed throughout the central and peripheral nervous systems. Missense mutations of the SLACK C-terminus have...

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Bibliografiske detaljer
Udgivet i:Neuroscience
Main Authors: Evely, Katherine M., Pryce, Kerri D., Bhattacharjee, Arin
Format: Artigo
Sprog:Inglês
Udgivet: 2017
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5479566/
https://ncbi.nlm.nih.gov/pubmed/28366665
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2017.03.035
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