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Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.

dc.contributor.authorBarc, Jen_US
dc.contributor.authorTadros, Ren_US
dc.contributor.authorGlinge, Cen_US
dc.contributor.authorChiang, DYen_US
dc.contributor.authorJouni, Men_US
dc.contributor.authorSimonet, Fen_US
dc.contributor.authorJurgens, SJen_US
dc.contributor.authorBaudic, Men_US
dc.contributor.authorNicastro, Men_US
dc.contributor.authorPotet, Fen_US
dc.contributor.authorOfferhaus, JAen_US
dc.contributor.authorWalsh, Ren_US
dc.contributor.authorChoi, SHen_US
dc.contributor.authorVerkerk, AOen_US
dc.contributor.authorMizusawa, Yen_US
dc.contributor.authorAnys, Sen_US
dc.contributor.authorMinois, Den_US
dc.contributor.authorArnaud, Men_US
dc.contributor.authorDuchateau, Jen_US
dc.contributor.authorWijeyeratne, YDen_US
dc.contributor.authorMuir, Aen_US
dc.contributor.authorPapadakis, Men_US
dc.contributor.authorCastelletti, Sen_US
dc.contributor.authorTorchio, Men_US
dc.contributor.authorOrtuño, CGen_US
dc.contributor.authorLacunza, Jen_US
dc.contributor.authorGiachino, DFen_US
dc.contributor.authorCerrato, Nen_US
dc.contributor.authorMartins, RPen_US
dc.contributor.authorCampuzano, Oen_US
dc.contributor.authorVan Dooren, Sen_US
dc.contributor.authorThollet, Aen_US
dc.contributor.authorKyndt, Fen_US
dc.contributor.authorMazzanti, Aen_US
dc.contributor.authorClémenty, Nen_US
dc.contributor.authorBisson, Aen_US
dc.contributor.authorCorveleyn, Aen_US
dc.contributor.authorStallmeyer, Ben_US
dc.contributor.authorDittmann, Sen_US
dc.contributor.authorSaenen, Jen_US
dc.contributor.authorNoël, Aen_US
dc.contributor.authorHonarbakhsh, Sen_US
dc.contributor.authorRudic, Ben_US
dc.contributor.authorMarzak, Hen_US
dc.contributor.authorRowe, MKen_US
dc.contributor.authorFederspiel, Cen_US
dc.contributor.authorLe Page, Sen_US
dc.contributor.authorPlacide, Len_US
dc.contributor.authorMilhem, Aen_US
dc.contributor.authorBarajas-Martinez, Hen_US
dc.contributor.authorBeckmann, B-Men_US
dc.contributor.authorKrapels, IPen_US
dc.contributor.authorSteinfurt, Jen_US
dc.contributor.authorWinkel, BGen_US
dc.contributor.authorJabbari, Ren_US
dc.contributor.authorShoemaker, MBen_US
dc.contributor.authorBoukens, BJen_US
dc.contributor.authorŠkorić-Milosavljević, Den_US
dc.contributor.authorBikker, Hen_US
dc.contributor.authorManevy, Fen_US
dc.contributor.authorLichtner, Pen_US
dc.contributor.authorRibasés, Men_US
dc.contributor.authorMeitinger, Ten_US
dc.contributor.authorMüller-Nurasyid, Men_US
dc.contributor.authorKORA-Study Groupen_US
dc.contributor.authorVeldink, JHen_US
dc.contributor.authorvan den Berg, LHen_US
dc.contributor.authorVan Damme, Pen_US
dc.contributor.authorCusi, Den_US
dc.contributor.authorLanzani, Cen_US
dc.contributor.authorRigade, Sen_US
dc.contributor.authorCharpentier, Een_US
dc.contributor.authorBaron, Een_US
dc.contributor.authorBonnaud, Sen_US
dc.contributor.authorLecointe, Sen_US
dc.contributor.authorDonnart, Aen_US
dc.contributor.authorLe Marec, Hen_US
dc.contributor.authorChatel, Sen_US
dc.contributor.authorKarakachoff, Men_US
dc.contributor.authorBézieau, Sen_US
dc.contributor.authorLondon, Ben_US
dc.contributor.authorTfelt-Hansen, Jen_US
dc.contributor.authorRoden, Den_US
dc.contributor.authorOdening, KEen_US
dc.contributor.authorCerrone, Men_US
dc.contributor.authorChinitz, LAen_US
dc.contributor.authorVolders, PGen_US
dc.contributor.authorvan de Berg, MPen_US
dc.contributor.authorLaurent, Gen_US
dc.contributor.authorFaivre, Len_US
dc.contributor.authorAntzelevitch, Cen_US
dc.contributor.authorKääb, Sen_US
dc.contributor.authorArnaout, AAen_US
dc.contributor.authorDupuis, J-Men_US
dc.contributor.authorPasquie, J-Len_US
dc.contributor.authorBillon, Oen_US
dc.contributor.authorRoberts, JDen_US
dc.contributor.authorJesel, Len_US
dc.contributor.authorBorggrefe, Men_US
dc.contributor.authorLambiase, PDen_US
dc.contributor.authorMansourati, Jen_US
dc.contributor.authorLoeys, Ben_US
dc.contributor.authorLeenhardt, Aen_US
dc.contributor.authorGuicheney, Pen_US
dc.contributor.authorMaury, Pen_US
dc.contributor.authorSchulze-Bahr, Een_US
dc.contributor.authorRobyns, Ten_US
dc.contributor.authorBreckpot, Jen_US
dc.contributor.authorBabuty, Den_US
dc.contributor.authorPriori, SGen_US
dc.contributor.authorNapolitano, Cen_US
dc.contributor.authorNantes Referral Center for inherited cardiac arrhythmiaen_US
dc.contributor.authorde Asmundis, Cen_US
dc.contributor.authorBrugada, Pen_US
dc.contributor.authorBrugada, Ren_US
dc.contributor.authorArbelo, Een_US
dc.contributor.authorBrugada, Jen_US
dc.contributor.authorMabo, Pen_US
dc.contributor.authorBehar, Nen_US
dc.contributor.authorGiustetto, Cen_US
dc.contributor.authorMolina, MSen_US
dc.contributor.authorGimeno, JRen_US
dc.contributor.authorHasdemir, Cen_US
dc.contributor.authorSchwartz, PJen_US
dc.contributor.authorCrotti, Len_US
dc.contributor.authorMcKeown, PPen_US
dc.contributor.authorSharma, Sen_US
dc.contributor.authorBehr, ERen_US
dc.contributor.authorHaissaguerre, Men_US
dc.contributor.authorSacher, Fen_US
dc.contributor.authorRooryck, Cen_US
dc.contributor.authorTan, HLen_US
dc.contributor.authorRemme, CAen_US
dc.contributor.authorPostema, PGen_US
dc.contributor.authorDelmar, Men_US
dc.contributor.authorEllinor, PTen_US
dc.contributor.authorLubitz, SAen_US
dc.contributor.authorGourraud, J-Ben_US
dc.contributor.authorTanck, MWen_US
dc.contributor.authorGeorge, ALen_US
dc.contributor.authorMacRae, CAen_US
dc.contributor.authorBurridge, PWen_US
dc.contributor.authorDina, Cen_US
dc.contributor.authorProbst, Ven_US
dc.contributor.authorWilde, AAen_US
dc.contributor.authorSchott, J-Jen_US
dc.contributor.authorRedon, Ren_US
dc.contributor.authorBezzina, CRen_US
dc.date.accessioned2023-09-06T15:47:56Z
dc.date.available2023-09-06T15:47:56Z
dc.date.issued2022-05en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/90507
dc.format.extent735 - ?en_US
dc.languageengen_US
dc.relation.ispartofNat Geneten_US
dc.titleAuthor Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.en_US
dc.typeArticle
dc.identifier.doi10.1038/s41588-022-01079-yen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/35474365en_US
pubs.issue5en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume54en_US


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