Home›Autosomal dominant disorders›羅曼諾-瓦爾德綜合症🌐中文EnglishDeutschEspañolFrançaisItalianoPolskiالعربية中文EntityQ724714· pop 8· linked from 231 articles羅曼諾-瓦爾德綜合症Also known as LQT, Romano-Ward syndrome, Romano-Ward syndrome (disorder), long Q-T syndrome, ROMANO-WARD syndromeHuman diseaseResearch424 papersSpectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.Circulation · 2000Mutation location and IKs regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region.European heart journal · 2021Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndrome.Circulation. Cardiovascular genetics · 2012The genetic basis of long QT and short QT syndromes: a mutation update.Human mutation · 2009Genetics of long-QT syndrome.Journal of human genetics · 2016via PubMedAvailable in 8 languagesEspañolFrançaisDeutschItalianoالعربيةBosnianPolskivia Wikidata sitelinks · CC0Connectionsangina pectorisEntityheart arrhythmiaEntityCategoriesAutosomal dominant disordersCardiac arrhythmiaChannelopathiesCommons link is the pagenameSource attributionSyndromes affecting the heart