SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome-Reference-Cited by-同舟云学术

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SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

Published:1995-03 Issue:5 Volume:80 Page:805-811
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Wang Qing,Shen Jiaxiang,Splawski Igor,Atkinson Donald,Li Zhizhong,Robinson Jennifer L,Moss Arthur J,Towbin Jeffrey A,Keating Mark T

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference42 articles.

1. Clinical relevance of cardiac arrhythmias generated by afterdepolarizations: role of M cells in the generation of U waves, triggered activity and torsade de pointes;Antzelevitch;J. Am. Coll. Cardiol.,1994

2. Steady-state TTX-sensitive (“window”) current in cardiac Purkinje fibres;Attwell;Pflügers Arch.,1979

3. An analysis of the time-relationships of electrocardiograms;Bazette;Heart,1920

4. A brain L-type calcium channel αl subunit gene (CCHL1A2) maps to mouse chromosome 14 and human chromosome 3;Chin;Genomics,1991

5. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome;Curran;Cell,1995

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4. Whole genome sequencing of families diagnosed with cardiac channelopathies reveals structural variants missed by whole exome sequencing;Journal of Human Genetics;2024-06-18

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