Characterisation of the human voltage-gated potassium channel gene, KCNA7, a candidate gene for inherited cardiac disorders, and its exclusion as cause of progressive familial heart block I (PFHBI).

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dc.contributor.authorBardien-Kruger S
dc.contributor.authorWulff H
dc.contributor.authorArieff Z
dc.contributor.authorBrink PA
dc.contributor.authorChandy KG
dc.contributor.authorCorfield VA
dc.date.accessioned2013-01-23T11:51:14Z
dc.date.available2013-01-23T11:51:14Z
dc.date.issued2002
dc.descriptionGesondheidswetenskappe
dc.descriptionInterne Geneeskunde
dc.descriptionPlease help us populate SUNScholar with the post print version of this article. It can be e-mailed to: scholar@sun.ac.za
dc.identifier.citationEuropean Journal of Human Genetics
dc.identifier.urihttp://hdl.handle.net/10019.1/74798
dc.publisherNATURE PUBLISHING GROUP, MACMILLAN BUILDING, 4 CRINAN ST, LONDON, ENGLAND, N19XW
dc.titleCharacterisation of the human voltage-gated potassium channel gene, KCNA7, a candidate gene for inherited cardiac disorders, and its exclusion as cause of progressive familial heart block I (PFHBI).
dc.typeJournal Articles (subsidised)
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