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Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano–Ward syndrome under double mutations and acquired long QT syndrome under heterozygote

Long Qt SyndromeRomano–ward SyndromeKcnh2 VariantGenetic DisorderGeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene IdentificationMedicineClinical Genetics