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KCNQ1 activates MTSS1. 1 / 1

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"Mutations in KCNQ1 cause the autosomal recessive Jervell and Lange-Nielsen syndrome [MIM 220400], characterized by SNHL and cardiac abnormalities (long QT syndrome) (Jervell and Lange-Nielsen, 1957; Neyroud et al., 1997)."

25663387

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IndraLab

Statements

KCNQ1 activates MTSS1. 1 / 1

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