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

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

Internet

http://scholarbank.nus.edu.sg/handle/10635/113329

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