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KCNQ1 activates translation. 1 / 1

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"To explain the presence of LQTS segregating with the t (11; 17) translocation in this family, we hypothesize that the translocation that interrupts KCNQ1 allow translation of an abnormal short allele that interferes in a dominant negative way with the normal isoform 1 of KCNQ1 in the heart (where this allele is not subject to parental imprint)."

23061425

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IndraLab

Statements

KCNQ1 activates translation. 1 / 1

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