Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia.
Long QT syndrome (LQT) is an autosomal dominant disorder that can cause sudden death from cardiac arrhythmias. We recently discovered that mutations in HERG, a K+-channel gene, cause chromosome 7-linked LQT. Heterologous expression of HERG in Xenopus oocytes revealed that HERG current was similar to...
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| Pubblicato in: | Proc Natl Acad Sci U S A |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
National Academy of Sciences
1996
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC39936/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8700910/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.93.5.2208 |
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