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Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia()
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| 發表在: | Int J Cardiol |
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| Main Authors: | , , , , , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2015
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5938092/ https://ncbi.nlm.nih.gov/pubmed/25791106 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijcard.2015.03.130 |
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