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Long QT syndrome: beyond the causal mutation
Congenital long QT syndrome (LQTS) is caused by single autosomal-dominant mutations in a gene encoding for a cardiac ion channel or an accessory ion channel subunit. These single mutations can cause life-threatening arrhythmias and sudden death in heterozygous mutation carriers. This recognition has...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Science Inc
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3779107/ https://ncbi.nlm.nih.gov/pubmed/23753525 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2013.254920 |
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