An RyR2 Mutation found in a family with a Short-coupled Variant of Torsade de Pointes

Saved in:

Bibliographic Details
Published in:	International journal of cardiology Vol. 227; pp. 367 - 369
Main Authors:	Kimura, Mai, Fujisawa, Taishi, Aizawa, Yoshiyasu, Matsuhashi, Noritaka, Ito, Shogo, Nakajima, Kazuaki, Kashimura, Shin, Kunitomi, Akira, Katsumata, Yoshinori, Nishiyama, Takahiko, Kimura, Takehiro, Nishiyama, Nobuhiro, Yuasa, Shinsuke, Takatsuki, Seiji, Kosaki, Kenjiro, Fukuda, Keiichi
Format:	Journal Article
Language:	English
Published:	Netherlands Elsevier B.V 15-01-2017
Subjects:	Adult Cardiovascular Female Humans Implantable cardioverter defibrillator Mutation - genetics Pedigree Ryanodine Receptor Calcium Release Channel - genetics Sudden death Torsade de pointes Torsades de Pointes - diagnosis Torsades de Pointes - genetics Torsades de Pointes - therapy Verapamil sudden death torsade de pointes implantable cardioverter defibrillator verapamil Verapamil Torsade de pointes Sudden death Implantable cardioverter defibrillator
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Description
Bibliography:	ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3
ISSN:	0167-5273 1874-1754
DOI:	10.1016/j.ijcard.2016.11.052