17199967

Source:http://linkedlifedata.com/resource/pubmed/id/17199967

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0018787, umls-concept:C0026882, umls-concept:C0039070, umls-concept:C0152035, umls-concept:C0205653, umls-concept:C0449450, umls-concept:C1335671, umls-concept:C1419779, umls-concept:C1631597, umls-concept:C1720824
pubmed:issue	24
pubmed:dateCreated	2007-1-3
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7513795
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Ion Channels, http://linkedlifedata.com/resource/pubmed/chemical/Ryanodine Receptor Calcium Release...
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0366-6999
pubmed:author	pubmed-author:ChanKwok-YinKY, pubmed-author:ChoiYuen-ChoiYC, pubmed-author:FongNai-ChungNC, pubmed-author:HuiYim-WoYW, pubmed-author:LamChing-WanCW, pubmed-author:MokNgai-ShingNS
pubmed:issnType	Print
pubmed:day	20
pubmed:volume	119
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2129-33
pubmed:meshHeading	pubmed-meshheading:17199967-Adolescent, pubmed-meshheading:17199967-Death, Sudden, Cardiac, pubmed-meshheading:17199967-Female, pubmed-meshheading:17199967-Humans, pubmed-meshheading:17199967-Ion Channels, pubmed-meshheading:17199967-Mutation, pubmed-meshheading:17199967-Ryanodine Receptor Calcium Release Channel, pubmed-meshheading:17199967-Syncope, pubmed-meshheading:17199967-Tachycardia, Ventricular
pubmed:year	2006
pubmed:articleTitle	Cardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope.
pubmed:affiliation	Department of Medicine & Geriatrics, Princess Margaret Hospital, Hong Kong, China. isaacmok@netvigator.com
pubmed:publicationType	Journal Article, Case Reports