H558R polymorphism in SCN5A is associated with Keshan disease and QRS prolongation in Keshan disease patients-Reference-Cited by-同舟云学术

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H558R polymorphism in SCN5A is associated with Keshan disease and QRS prolongation in Keshan disease patients

Published:2014 Issue:3 Volume:13 Page:6569-6576
ISSN:1676-5680
Container-title:Genetics and Molecular Research
language:
Short-container-title:Genet. Mol. Res.

Author:

Jiang S.,Li F.L.,Dong Q.,Liu H.W.,Fang C.F.,Shu C.,Cheng H.,Cui J.,Ma H.X.,Chen D.Q.,Li H.

Publisher

Genetics and Molecular Research

Subject

Genetics,Molecular Biology,General Medicine

Link

http://www.funpecrp.com.br/gmr/year2014/vol13-3/pdf/gmr2607.pdf

Cited by 7 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. Progress in selenium and genetics associated with Keshan disease;Journal of Trace Elements and Minerals;2024-03

2. Malezya'daki Malaylar Arasında İrritabl Bağırsak Sendromu (IBS) ile ilişkili Tek Nükleotid Polimorfizmlerinin Genotip ve Alel Frekansları;Düzce Tıp Fakültesi Dergisi;2023-08-30

3. SCN5A gene variants as potential markers of the progression of chronic chagasic cardiac alterations;Parasitology International;2021-02

4. Core Principles in Nutrition: Nutrient Needs, Metabolism, and Potential Influences on Infectious Diseases;Nutrition and Infectious Diseases;2020-12-11

5. The epidemiological status, environmental and genetic factors in the etiology of Keshan disease;Cardiovascular Endocrinology & Metabolism;2020-06-19

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