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KCNQ1 activates JLN1. 1 / 1

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"Homozygous or compound heterozygous mutation in either KCNQ1 or KCNE1 (minK) causes the Jervell and Lange-Nielsen autosomal recessive form of the disease (JLN1 and JLN2, respectively), which is characterized by cardiac phenotype (long QT interval and susceptibility to ventricular arrhythmia) and sensorineural deafness."

20890437

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KCNQ1 activates JLN1. 1 / 1

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