Functionally Aberrant Mutant KCNQ1 With Intermediate Heterozygous and Homozygous Phenotypes
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
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Cited by 2 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. Compound Heterozygous KCNQ1 Mutations Causing Recessive Romano–Ward Syndrome: Functional Characterization by Mutant Co-expression;Frontiers in Cardiovascular Medicine;2021-02-22
2. Extensive Diversity of Molecular Mechanisms Underlying the Congenital Long QT Syndrome Type 1;Canadian Journal of Cardiology;2018-09
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