A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype-Reference-Cited by-同舟云学术

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A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype

Published:2001-06-26 Issue:9 Volume:79 Page:504-509
ISSN:0946-2716
Container-title:Journal of Molecular Medicine
language:en
Short-container-title:J Mol Med

Author:

Schulze-Bahr Eric,Schwarz Martin,Hoffmann Susanne,Wedekind Horst,Funke Harald,Haverkamp Wilhelm,Breithardt Günter,Pongs Olaf,Isbrandt Dirk

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Drug Discovery,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s001090100249.pdf

Cited by 27 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. Genetic homozygosity in a diverse population: An experience of long QT syndrome;International Journal of Cardiology;2020-10

2. Clinical and functional reappraisal of alleged type 5 long QT syndrome: Causative genetic variants in the KCNE1-encoded minK β-subunit;Heart Rhythm;2020-06

3. An International Multicenter Evaluation of Type 5 Long QT Syndrome;Circulation;2020-02-11

4. Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange‐Nielsen Syndrome and Romano‐Ward Syndrome;Human Mutation;2018-12-12

5. The genetic architecture of long QT syndrome: A critical reappraisal;Trends in Cardiovascular Medicine;2018-10

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