IndraLab

Statements



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"SCN5A variants may cause unpredictable hNa v 1.5 response to antiarrythmic agents."

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"Subsequently, genetic testing identified 1 base pair deletion mutation in the SCN5A, which causes a frame shift and truncates the hNa v 1.5 starting at amino acid 1397, where truncation in the domain [MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"