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Pathophysiology of KCNQ channels: neonatal epilepsy and progressive deafness

Item Type:Article
Title:Pathophysiology of KCNQ channels: neonatal epilepsy and progressive deafness
Creators Name:Jentsch, T.J. and Schroeder, B.C. and Kubisch, C. and 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 (U.S.A.)
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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