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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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dc.contributor.authorRichards, M.-
dc.contributor.authorHeron, S.-
dc.contributor.authorSpendlove, H.-
dc.contributor.authorScheffer, I.-
dc.contributor.authorGrinton, B.-
dc.contributor.authorBerkovic, S.-
dc.contributor.authorMulley, J.-
dc.contributor.authorDavy, A.-
dc.date.issued2004-
dc.identifier.citationJournal of Medical Genetics, 2004; 41(3):WWW 1-WWW 6-
dc.identifier.issn0022-2593-
dc.identifier.issn1468-6244-
dc.identifier.urihttp://hdl.handle.net/2440/3055-
dc.descriptionCopyright © 2004 by the BMJ Publishing Group Ltd.-
dc.description.statementofresponsibilityM C Richards, S E Heron, H E Spendlove, I E Scheffer, B Grinton, S F Berkovic, J C Mulley, A Davy-
dc.language.isoen-
dc.publisherBritish Med Journal Publ Group-
dc.source.urihttp://dx.doi.org/10.1136/jmg.2003.013938-
dc.subjectbenign familial neonatal seizures-
dc.subjectcalmodulin-
dc.subjectepilepsy-
dc.subjectKCNQ2-
dc.subjectpotassium channel-
dc.titleNovel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction-
dc.typeJournal article-
dc.identifier.doi10.1136/jmg.2003.013938-
pubs.publication-statusPublished-
dc.identifier.orcidHeron, S. [0000-0001-8759-6748]-
Appears in Collections:Aurora harvest 6
Molecular and Biomedical Science publications

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