IndraLab

Statements

PSMD4 activates KCNQ1. 3 / 3
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reach
"A whole-genome scan with polymorphic microsatellite markers and linkage analysis mapped the AF susceptibility loci on human chromosomes 10q22, 6q14-16, 11p15.5, 5p15, 10p11-q21, and 5p13, for which the AF causing mutations in 2 genes, KCNQ1 on chromosome 11p15.5 and NUP155 on chromosome 5p13, were identified and functionally characterized."
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"The initial AF causing mutation in KCNQ1 was identified by a positional candidate gene approach, whereas other ion-channel genes associated with AF were identified by the candidate gene approach in sp[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
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"Following genome-wide linkage analysis with polymorphic genetic markers, specific susceptibility loci for AF have been mapped to human chromosomes 10q22, 6q14-16, 11p15.5, 5p15, 10p11-q21, and 5p13, and AF causing mutations in two genes, KCNQ1 on chromosome 11p15.5 and NUP155 on chromosome 5p13, have been identified and characterized."
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