Article: Cardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope

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TitleCardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope
AuthorsMok, NS1
Lam, CW2
Fong, NC1
Hui, YW1
Choi, YC1
Chan, KY1
Issue Date2006
PublisherZhonghua Yixuehui. The Journal's web site is located at http://www.cmj.org/
CitationChinese Medical Journal, 2006, v. 119 n. 24, p. 2129-2133 [How to Cite?]
ISSN0366-6999
2011 Impact Factor: 0.864
2011 SCImago Journal Rankings: 0.077
ISI Accession Number IDWOS:000243090400018
ReferencesReferences in Scopus
DC Field
Value
dc.contributor.authorMok, NS
dc.contributor.authorLam, CW
dc.contributor.authorFong, NC
dc.contributor.authorHui, YW
dc.contributor.authorChoi, YC
dc.contributor.authorChan, KY
dc.date.accessioned2012-05-29T06:13:18Z
dc.date.available2012-05-29T06:13:18Z
dc.date.issued2006
dc.description.natureLink_to_subscribed_fulltext
dc.identifier.citationChinese Medical Journal, 2006, v. 119 n. 24, p. 2129-2133 [How to Cite?]
dc.identifier.epage2133
dc.identifier.isiWOS:000243090400018
dc.identifier.issn0366-6999
2011 Impact Factor: 0.864
2011 SCImago Journal Rankings: 0.077
dc.identifier.issue24
dc.identifier.pmid17199967
dc.identifier.scopuseid_2-s2.0-33845901494
dc.identifier.spage2129
dc.identifier.urihttp://hdl.handle.net/10722/148496
dc.identifier.volume119
dc.languageeng
dc.publisherZhonghua Yixuehui. The Journal's web site is located at http://www.cmj.org/
dc.publisher.placeChina
dc.relation.ispartofChinese Medical Journal
dc.relation.referencesReferences in Scopus
dc.subject.meshAdolescent
dc.subject.meshDeath, Sudden, Cardiac - Etiology
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshIon Channels - Physiology
dc.subject.meshMutation
dc.subject.meshRyanodine Receptor Calcium Release Channel - Genetics
dc.subject.meshSyncope - Etiology
dc.subject.meshTachycardia, Ventricular - Genetics
dc.titleCardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope
dc.typeArticle
Author Affiliations
  1. Princess Margaret Hospital Hong Kong
  2. Prince of Wales Hospital Hong Kong