Maternal mosaicism in long QT syndrome due to a pathogenic variant in KCNH2

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dc.contributor.authorSawyer, Briana L.
dc.contributor.authorTristani-Firouzi, Martin
dc.contributor.authorWells, Layne E.
dc.contributor.authorVatta, Matteo
dc.contributor.authorEtheridge, Susan P.
dc.contributor.departmentMedical and Molecular Genetics, School of Medicineen_US
dc.date.accessioned2022-07-18T10:55:21Z
dc.date.available2022-07-18T10:55:21Z
dc.date.issued2020-11-16
dc.eprint.versionFinal published versionen_US
dc.identifier.citationSawyer BL, Tristani-Firouzi M, Wells LE, Vatta M, Etheridge SP. Maternal mosaicism in long QT syndrome due to a pathogenic variant in KCNH2. HeartRhythm Case Rep. 2020;7(2):74-78. Published 2020 Nov 16. doi:10.1016/j.hrcr.2020.11.006en_US
dc.identifier.urihttps://hdl.handle.net/1805/29602
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.hrcr.2020.11.006en_US
dc.relation.journalHeartRhythm Case Reportsen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourcePMCen_US
dc.subjectGenetic testingen_US
dc.subjectGonosomal mosaicismen_US
dc.subjectInherited arrhythmiaen_US
dc.subjectIon channelen_US
dc.subjectLong QT syndromeen_US
dc.subjectMosaicismen_US
dc.titleMaternal mosaicism in long QT syndrome due to a pathogenic variant in KCNH2en_US
dc.typeArticleen_US
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