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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/3055
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Type: Journal article
Title: Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction
Author: Richards, M.
Heron, S.
Spendlove, H.
Scheffer, I.
Grinton, B.
Berkovic, S.
Mulley, J.
Davy, A.
Citation: Journal of Medical Genetics, 2004; 41(3):WWW 1-WWW 6
Publisher: British Med Journal Publ Group
Issue Date: 2004
ISSN: 0022-2593
1468-6244
Statement of
Responsibility: 		M C Richards, S E Heron, H E Spendlove, I E Scheffer, B Grinton, S F Berkovic, J C Mulley, A Davy
Keywords: benign familial neonatal seizures
calmodulin
epilepsy
KCNQ2
potassium channel
Description: Copyright © 2004 by the BMJ Publishing Group Ltd.
DOI: 10.1136/jmg.2003.013938
Published version: http://dx.doi.org/10.1136/jmg.2003.013938
Appears in Collections:Aurora harvest 6
Molecular and Biomedical Science publications

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