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Bifid T waves on the ECG and genetic variation in calcium channel voltage-dependent beta 2 subunit gene (CACNB2) in acute Kawasaki disease.

Jun OyamadaChisato ShimizuJihoon KimMatthew R WilliamsEileen PngMartin L HibberdAdriana H TremouletJames C PerryJane C Burns
Published in: Congenital heart disease (2018)
This genotype/phenotype association study uncovered a variant in CACNB2 that may be associated with both KD susceptibility and bifid T waves, a novel signature of altered myocardial repolarization. The present study combined with published reports suggests that genetic variants in calcium channels and intracellular calcium signaling play a prominent role in shaping susceptibility to KD.
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