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Disease Modifiers of Inherited SCN5A Channelopathy
To date, a large number of mutations in SCN5A, the gene encoding the pore-forming α-subunit of the primary cardiac Na(+) channel (Na(V)1.5), have been found in patients presenting with a wide range of ECG abnormalities and cardiac syndromes. Although these mutations all affect the same Na(V)1.5 chan...
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| 發表在: | Front Cardiovasc Med |
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| Main Authors: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Frontiers Media S.A.
2018
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6174200/ https://ncbi.nlm.nih.gov/pubmed/30327767 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcvm.2018.00137 |
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