Pathophysiology of KCNQ channels: neonatal epilepsy and progressive deafness

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Item Type:	Article
Title:	Pathophysiology of KCNQ channels: neonatal epilepsy and progressive deafness
Creators Name:	Jentsch, T.J., Schroeder, B.C., Kubisch, C., Friedrich, T. and Stein, V.
Keywords:	Human Chromosomes Pair 20, Human Chromosomes Pair 8, Deafness, Disease Progression, Benign Neonatal Epilepsy, Dominant Genes, Outer Auditory Hair Cells, Mutation, Potassium Channels
Source:	Epilepsia
ISSN:	0013-9580
Publisher:	Lippincott Williams & Wilkins
Volume:	41
Number:	8
Page Range:	1068-1069
Date:	August 2000
Official Publication:	https://doi.org/10.1111/j.1528-1157.2000.tb00302.x
PubMed:	View item in PubMed

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