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A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect
- Correspondence to: Y-T Chen Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan; chen0010{at}ibms.sinica.edu.tw
Citation
A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect
Publication history
- Received March 7, 2006
- Accepted April 13, 2006
- Revised April 11, 2006
- First published May 17, 2006.
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April 27, 2016
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Copyright 2006 Journal of Medical Genetics