A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family

10.1055/s-2000-15290

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Bibliographic Details
Main Authors:	Lee, W.L., Biervert, C., Hallmann, K., Tay, A., Dean, J.C.S., Steinlein, O.K.
Other Authors:	PAEDIATRICS
Format:	Article
Published:	2014
Subjects:	Epilepsy Gene mutation Potassium channel
Online Access:	http://scholarbank.nus.edu.sg/handle/10635/113329
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Institution:	National University of Singapore

Description
Summary:	10.1055/s-2000-15290

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