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

TitleCardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope
Authors
Mok, NSLam, CWFong, NCHui, YWChoi, YCChan, KY
KeywordsCardiac ryanodine receptor
Catecholaminergic polymorphic ventricular tachycardia
Chinese
Sudden death
Issue Date2006
PublisherChinese Medical Association. The Journal's web site is located at http://www.cmj.org/
Citation
Chinese Medical Journal, 2006, v. 119 n. 24, p. 2129-2133 How to Cite?
DOI: http://dx.doi.org/10.1097/00029330-200612020-00018
Persistent Identifierhttp://hdl.handle.net/10722/148496
ISSN
0366-6999
2021 Impact Factor: 6.133
2020 SCImago Journal Rankings: 0.537
ISI Accession Number ID
WOS:000243090400018
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorMok, NSen_US
dc.contributor.authorLam, CWen_US
dc.contributor.authorFong, NCen_US
dc.contributor.authorHui, YWen_US
dc.contributor.authorChoi, YCen_US
dc.contributor.authorChan, KYen_US
dc.date.accessioned2012-05-29T06:13:18Z-
dc.date.available2012-05-29T06:13:18Z-
dc.date.issued2006en_US
dc.identifier.citationChinese Medical Journal, 2006, v. 119 n. 24, p. 2129-2133en_US
dc.identifier.issn0366-6999en_US
dc.identifier.urihttp://hdl.handle.net/10722/148496-
dc.languageengen_US
dc.publisherChinese Medical Association. The Journal's web site is located at http://www.cmj.org/en_US
dc.relation.ispartofChinese Medical Journalen_US
dc.subjectCardiac ryanodine receptor-
dc.subjectCatecholaminergic polymorphic ventricular tachycardia-
dc.subjectChinese-
dc.subjectSudden death-
dc.subject.meshAdolescenten_US
dc.subject.meshDeath, Sudden, Cardiac - Etiologyen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshIon Channels - Physiologyen_US
dc.subject.meshMutationen_US
dc.subject.meshRyanodine Receptor Calcium Release Channel - Geneticsen_US
dc.subject.meshSyncope - Etiologyen_US
dc.subject.meshTachycardia, Ventricular - Geneticsen_US
dc.titleCardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncopeen_US
dc.typeArticleen_US
dc.identifier.emailLam, CW:ching-wanlam@pathology.hku.hken_US
dc.identifier.authorityLam, CW=rp00260en_US
dc.description.naturelink_to_OA_fulltexten_US
dc.identifier.doi10.1097/00029330-200612020-00018-
dc.identifier.pmid17199967-
dc.identifier.scopuseid_2-s2.0-33845901494en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-33845901494&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume119en_US
dc.identifier.issue24en_US
dc.identifier.spage2129en_US
dc.identifier.epage2133en_US
dc.identifier.isiWOS:000243090400018-
dc.publisher.placeChinaen_US
dc.identifier.issnl0366-6999-

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