Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes

Author:

Shigemizu Daichi,Aiba Takeshi,Nakagawa Hidewaki,Ozaki Kouichi,Miya Fuyuki,Satake Wataru,Toda Tatsushi,Miyamoto Yoshihiro,Fujimoto Akihiro,Suzuki Yutaka,Kubo Michiaki,Tsunoda Tatsuhiko,Shimizu Wataru,Tanaka Toshihiro

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference53 articles.

1. The QT syndromes: long and short;H Morita;Lancet,2008

2. Prevalence of the congenital long-QT syndrome;PJ Schwartz;Circulation,2009

3. Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C, Linked to Autosomal Dominant Long QT Syndrome;NJ Boczek;Circulation Cardiovascular genetics,2013

4. Exome sequencing and the genetic basis of complex traits;A Kiezun;Nature genetics,2012

5. Genetic diagnosis by whole exome capture and massively parallel DNA sequencing;M Choi;Proc Natl Acad Sci U S A,2009

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