IndraLab

Statements


CACNA1C activates BRS3. 2 / 2
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"Mutations in CACNA1C, CACNB2 and CACNA2D1 can cause BrS3, BrS4 and BrS9, respectively [96,97]."

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"Thus, BrS3, caused by the mutation in CACNA1C, such as p.A39V, p.G490R, p.E1829 _ Q1833 duplication, and p.E850 deletion, also known as SQT4; and BrS4, caused by CACNB2 p.S481L mutation, is also known as SQT5 [98]."