Long QT syndrome with compound mutations is associated with a more severe phenotype: A Japanese multicenter study-Reference-Cited by-同舟云学术

Long QT syndrome with compound mutations is associated with a more severe phenotype: A Japanese multicenter study

Published:2010-10 Issue:10 Volume:7 Page:1411-1418
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Itoh Hideki,Shimizu Wataru,Hayashi Kenshi,Yamagata Kenichiro,Sakaguchi Tomoko,Ohno Seiko,Makiyama Takeru,Akao Masaharu,Ai Tomohiko,Noda Takashi,Miyazaki Aya,Miyamoto Yoshihiro,Yamagishi Masakazu,Kamakura Shiro,Horie Minoru

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference33 articles.

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4. Mutation of an A-kinase-anchoring protein causes long-QT syndrome;Chen;Proc Natl Acad Sci U S A,2007

5. Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex;Ueda;Proc Natl Acad Sci U S A,2008

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