1218Double mutations in RYR2 cause severe phenotype of catecholaminergic polymorphic ventricular tachycardia. (29th August 2017)

Record Type:: Journal Article
Title:: 1218Double mutations in RYR2 cause severe phenotype of catecholaminergic polymorphic ventricular tachycardia. (29th August 2017)
Main Title:: 1218Double mutations in RYR2 cause severe phenotype of catecholaminergic polymorphic ventricular tachycardia
Authors:: Takayama, K.
Ohno, S.
Fukumoto, D.
Wada, Y.
Ichikawa, M.
Fukuyama, M.
Itoh, H.
Horie, M.
Abstract:
Is Part Of:: European heart journal. Volume 38(2017)Supplement 1
Journal:: European heart journal
Issue:: Volume 38(2017)Supplement 1
Issue Display:: Volume 38, Issue 1 (2017)
Year:: 2017
Volume:: 38
Issue:: 1
Issue Sort Value:: 2017-0038-0001-0000
Page Start:
Page End:
Publication Date:: 2017-08-29
Subjects:: Cardiology -- Periodicals
Heart -- Diseases -- Periodicals
616.12005
Journal URLs:: http://eurheartj.oxfordjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗
DOI:: 10.1093/eurheartj/ehx502.1218 ↗
Languages:: English
ISSNs:: 0195-668X
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3829.717500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 12238.xml