Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation
| Autor: | Park, Ji Kwon, Martin, Lisa J., Zhang, Xue, Jegga, Anil G., Benson, D. Woodrow |
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| Zdroj: | In Heart Rhythm July 2012 9(7):1090-1096 |
| Databáze: | ScienceDirect |
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