Genomic organization and mutational analysis of HERG , a gene responsible for familial long QT syndrome-Reference-Cited by-同舟云学术

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Genomic organization and mutational analysis of HERG , a gene responsible for familial long QT syndrome

Published:1998-04-23 Issue:4 Volume:102 Page:435-439
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Itoh Toshio,Tanaka T.,Nagai Ryozo,Kamiya Tetsuro,Sawayama Toshitami,Nakayama Toshio,Tomoike Hitonobu,Sakurada Harumizu,Yazaki Yoshio,Nakamura Yusuke

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390050717.pdf

Cited by 70 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Racial Disparities in Ion Channelopathies and Inherited Cardiovascular Diseases Associated With Sudden Cardiac Death;Journal of the American Heart Association;2022-03-15

2. A cardiac sodium channel mutation associated with epinephrine‐induced marked QT‐prolongation;Journal of Cardiovascular Electrophysiology;2020-05-25

3. R534C mutation in hERG causes a trafficking defect in iPSC-derived cardiomyocytes from patients with type 2 long QT syndrome;Scientific Reports;2019-12

4. Potassium Channel Mutations and Human Disease;Molecular, Genetic, and Nutritional Aspects of Major and Trace Minerals;2017

5. Negative-dominance phenomenon with genetic variants of the cardiac sodium channel Na v 1.5;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2016-07

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