Clinical Spectrum of <i>KCNA1</i> Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity

Clinical Spectrum of <i>KCNA1</i> Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity

Mutations in the <i>KCNA1</i> gene, which encodes voltage-gated Kv1.1 potassium channel α-subunits, cause a variety of human diseases, complicating simple genotype–phenotype correlations in patients. <i>KCNA1</i> mutations are primarily associated with a rare neurological mov...

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Bibliographic Details
Main Authors: Kelsey Paulhus, Lauren Ammerman, Edward Glasscock
Format: Article
Language:English
Published: MDPI AG 2020-04-01
Series:International Journal of Molecular Sciences
Subjects:
episodic ataxia
epilepsy
<i>KCNA1</i>
Kv1.1
Online Access:https://www.mdpi.com/1422-0067/21/8/2802

Internet

https://www.mdpi.com/1422-0067/21/8/2802

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