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ABCC9 is a Novel Brugada and Early Repolarization Syndrome Susceptibility Gene
BACKGROUND: Genetic defects in KCNJ8, encoding the Kir6.1 subunit of the ATP-sensitive K(+) channel (I(K-ATP)), have previously been associated with early repolarization (ERS) and Brugada (BrS) syndromes. Here we test the hypothesis genetic variants in ABCC9, encoding the ATP-binding cassette transp...
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2014
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3947869/ https://ncbi.nlm.nih.gov/pubmed/24439875 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijcard.2013.12.084 |
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