IndraLab

Statements


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"Some SCN5A mutations are associated with both BrS1 and LQT3."

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"BrS1 is associated with mutations in SCN5A."

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"Although many studies have been published on the prevalence and biophysical impacts of the arrhythmogenic variant E1784K ( xref ; xref ; xref ; xref ), until recently little was known about the mechanism by which E1784K, and other C-terminal variants associated with BrS1 and LQT3, lead to altered inactivation ( xref ; xref ; xref ; xref )."