Identification of rare heterozygous linkage R965C‐R1309H mutations in the pore‐forming region of SCN5A gene associated with complex arrhythmia-Reference-Cited by-同舟云学术

Identification of rare heterozygous linkage R965C‐R1309H mutations in the pore‐forming region of SCN5A gene associated with complex arrhythmia

Published:2021-03-25 Issue: Volume: Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Lin Yubi¹²,Qin Jiading¹^ORCID,Shen Yuhui¹³,Huang Jiana⁴,Zhang Zuoquan¹,Zhu ZhiLing¹,Lu Huifang¹,Huang Yin¹,Yin Yuelan¹,Wang Ani¹,Jin Lizi¹,Hu Zhenyu¹,Lin Xiufang¹,Jiang Bin¹³

Affiliation:

1. The Cardiovascular Center Department of Cardiology Interventional Medical Center Guangdong Provincial Key Laboratory of Biomedical Imaging and Guangdong Provincial Engineering Research Center of Molecular Imaging The Fifth Affiliated HospitalSun Yat‐sen University Zhuhai China

2. Guangdong Provincial People's Hospital Guangdong Academy of Medical Sciences Guangdong Cardiovascular InstituteGuangzhou China

3. Guangdong Province Key Laboratory of Brain Function and Disease Zhongshan School of Medicine Sun Yat‐sen University Guangzhou China

4. Reproductive Medicine Center The Sixth Affiliated Hospital of Sun Yat‐Sen University Guangzhou China

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1613

Reference10 articles.

1. Genetics of Sudden Cardiac Death

2. Modulation of Nav1.5 Channel Function by an Alternatively Spliced Sequence in the DII/DIII Linker Region

3. Cardiac Na Channels

4. Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations

5. Genetics of inherited cardiomyopathy

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