IndraLab

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Mutated KCNQ1 decreases the amount of Lys-Ser. 1 / 1

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reach

"The above studies suggest that loss-of-function in I Ks caused by KCNQ1 mutation not only can predispose patients to congenital LQT1, but can be also associated with acquired LQT1."

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IndraLab

Statements

Mutated KCNQ1 decreases the amount of Lys-Ser. 1 / 1

INDRA sources:

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