Calmodulin mutations can underlie the phenotype of long QT syndrome variant 1
- PMID: 37555447
- DOI: 10.1113/JP285220
Calmodulin mutations can underlie the phenotype of long QT syndrome variant 1
Keywords: CALM-2; IKS potassium channel; calmodulin; long QT syndrome.
Comment on
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Long QT syndrome-associated calmodulin variants disrupt the activity of the slowly activating delayed rectifier potassium channel.J Physiol. 2023 Sep;601(17):3739-3764. doi: 10.1113/JP284994. Epub 2023 Jul 10. J Physiol. 2023. PMID: 37428651 Free PMC article.
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