Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family
Open Access
- 1 January 2016
- journal article
- case report
- Published by Japanese Society of Internal Medicine in Internal Medicine
- Vol. 55 (3) , 259-262
Abstract
Japan's largest platform for academic e-journals: J-STAGE is a full text database for reviewed academic papers published by Japanese societiesKeywords
This publication has 15 references indexed in Scilit:
- Sex Hormones and the QT Interval: A ReviewJournal of Women's Health, 2012
- Genotype-Phenotype Aspects of Type 2 Long QT SyndromeJACC, 2009
- Influence of Menstrual Cycle on QT Interval DynamicsPacing and Clinical Electrophysiology, 2006
- Clinical and electrophysiological characterization of a novel mutation R863X in HERG C-terminus associated with long QT syndromeJournal of Molecular Medicine, 2004
- Structural and Functional Role of the Extracellular S5-P Linker in the HERG Potassium ChannelJournal of General Physiology, 2002
- Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2Clinical Genetics, 2000
- Influence of the Genotype on the Clinical Course of the Long-QT SyndromeNew England Journal of Medicine, 1998
- Age- and Sex-Related Differences in Clinical Manifestations in Patients With Congenital Long-QT SyndromeCirculation, 1998
- Skeletal and Sexual Maturation in Japanese ChildrenClinical Pediatric Endocrinology, 1993
- Alteration of ionic selectivity of a K+ channel by mutation of the H5 regionNature, 1991