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Pharmacological targeting of long QT mutant sodium channels.

The congenital long QT syndrome (LQTS) is an inherited disorder characterized by a delay in cardiac cellular repolarization leading to cardiac arrhythmias and sudden death often in young people. One form of the disease (LQT3) involves mutations in the voltage-gated cardiac sodium channel. The potent...

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Dades bibliogràfiques
Publicat a:J Clin Invest
Autors principals: Wang, D W, Yazawa, K, Makita, N, George, A L, Bennett, P B
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 1997
Matèries:
Accés en línia:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC507992/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9120016/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI119335
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