KCNQ2- and KCNQ3-associated epilepsy /

"KCNQ2 and KCNQ3 encode subunits (KV7.2, KV7.3) that combine to form a voltagegated potassium ion (K ) channel responsible for generating an ionic current (M-current) important for controlling activity in the nervous system. Pathogenic variants in both genes are associated with a spectrum of ge...

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Bibliographic Details

Corporate Author:	Cambridge University Press
Other Authors:	Weckhuysen, Sarah (Editor), George, Alfred L. (Editor)
Format:	eBook
Language:	English
Published:	Cambridge, United Kingdom ; New York, NY : Cambridge University Press, 2022.
Series:	Elements in genetics in epilepsy.
Subjects:	Infantile spasms > Genetic aspects. Infantile spasms > Etiology. Epilepsy > Genetic aspects. Epilepsy > Etiology. Epilepsy, Benign Neonatal > genetics Epilepsy, Benign Neonatal > etiology KCNQ2 Potassium Channel > metabolism KCNQ3 Potassium Channel > metabolism Syndrome des spasmes en flexion > Aspect génétique. Syndrome des spasmes en flexion > Étiologie. Epilepsy > Etiology Epilepsy > Genetic aspects Electronic books.
Online Access:	Connect to the full text of this electronic book