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Physiological genomics identifies genetic modifiers of long QT syndrome type 2 severity
Congenital long QT syndrome (LQTS) is an inherited channelopathy associated with life-threatening arrhythmias. LQTS type 2 (LQT2) is caused by mutations in KCNH2, which encodes the potassium channel hERG. We hypothesized that modifier genes are partly responsible for the variable phenotype severity...
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| Publicado no: | J Clin Invest |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5824853/ https://ncbi.nlm.nih.gov/pubmed/29431731 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI94996 |
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