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Paper Details

Clinically Relevant <i>KCNQ1</i> Variants Causing KCNQ1-KCNE2 Gain-of-Function Affect the Ca<sup>2+</sup> Sensitivity of the Channel.
Int J Mol Sci
0
2022
Ca, Dominant variants, K, KCNE2, KCNQ1, KCNQ1 channelopathy, KCNQ1 mutant channels, KCNQ1 mutants, P369L, Q1E2, R116L, V185M, V185M-Q1E2, allelic disorder, calcified calmodulin, calmodulin, cardiac arrhythmia syndromes, genetic defect, gingival fibromatosis, gingival overgrowth, mutant KCNQ1 channels, pituitary hormone deficiency, resting, resting Q1E2, wild-type KCNQ1, wild-type Q1E2 channels
Author NameAffiliation
Denise HornCharite-Universitatsmedizin Berlin, Corporate Member of Freie Universitat Berlin, Humboldt Universitat zu Berlin and Berlin Institute of Health
Kerstin KutscheInstitute of Human Genetics, University Medical Center Hamburg-Eppendorf
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