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Functional study of a KCNH2 mutant: Novel insights on the pathogenesis of the LQT2 syndrome
The K(+) voltage‐gated channel subfamily H member 2 (KCNH2) transports the rapid component of the cardiac delayed rectifying K(+) current. The aim of this study was to characterize the biophysical properties of a C‐terminus‐truncated KCNH2 channel, G1006fs/49 causing long QT syndrome type II in hete...
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| Publicado no: | J Cell Mol Med |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6714209/ https://ncbi.nlm.nih.gov/pubmed/31361068 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.14521 |
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