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Article: SCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups

TitleSCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups
Authors
Baruteau, AEKyndt, FBehr, ERVink, ASLachaud, MJoong, ASchott, JJHorie, MDenjoy, ICrotti, LShimizu, WBos, JMSStephenson, EAWong, LAbrams, DJDavis, AMWinbo, ADubin, AMSanatani, SLiberman, LKaski, JPRudic, BKwok, SYRieubland, CTfelt-Hansen, JVan Hare, GFGuyomarc'h-Delasalle, BBlom, NAWijeyeratne, YDGourraud, JDLe Marec, HOzawa, JFressart, VLupoglazoff, JMDagradi, FSpazzolini, CAiba, TTester, DJZahavich, LABeausejour-Ladouceur, VJadhav, MSkinner, JRFranciosi, SKrahn, ADAbdelsayed, MRuben, PCYung, TCAckerman, MJWilde, AASchwartz, PJProbst, V
KeywordsBrugada syndrome
Genotype-phenotype correlation
Long QT syndrome
Progressive cardiac conduction disorders
SCN5A
Sodium channelopathy
Issue Date2018
Citation
European Heart Journal, 2018, v. 39, p. 2879-2887 How to Cite?
DOI: http://dx.doi.org/10.1093/eurheartj/ehy412
Persistent Identifierhttp://hdl.handle.net/10722/260555
ISSN
0195-668X
2023 Impact Factor: 37.6
2023 SCImago Journal Rankings: 4.091
ISI Accession Number ID
WOS:000442981200009

 

DC FieldValueLanguage
dc.contributor.authorBaruteau, AE-
dc.contributor.authorKyndt, F-
dc.contributor.authorBehr, ER-
dc.contributor.authorVink, AS-
dc.contributor.authorLachaud, M-
dc.contributor.authorJoong, A-
dc.contributor.authorSchott, JJ-
dc.contributor.authorHorie, M-
dc.contributor.authorDenjoy, I-
dc.contributor.authorCrotti, L-
dc.contributor.authorShimizu, W-
dc.contributor.authorBos, JM-
dc.contributor.authorSStephenson, EA-
dc.contributor.authorWong, L-
dc.contributor.authorAbrams, DJ-
dc.contributor.authorDavis, AM-
dc.contributor.authorWinbo, A-
dc.contributor.authorDubin, AM-
dc.contributor.authorSanatani, S-
dc.contributor.authorLiberman, L-
dc.contributor.authorKaski, JP-
dc.contributor.authorRudic, B-
dc.contributor.authorKwok, SY-
dc.contributor.authorRieubland, C-
dc.contributor.authorTfelt-Hansen, J-
dc.contributor.authorVan Hare, GF-
dc.contributor.authorGuyomarc'h-Delasalle, B-
dc.contributor.authorBlom, NA-
dc.contributor.authorWijeyeratne, YD-
dc.contributor.authorGourraud, JD-
dc.contributor.authorLe Marec, H-
dc.contributor.authorOzawa, J-
dc.contributor.authorFressart, V-
dc.contributor.authorLupoglazoff, JM-
dc.contributor.authorDagradi, F-
dc.contributor.authorSpazzolini, C-
dc.contributor.authorAiba, T-
dc.contributor.authorTester, DJ-
dc.contributor.authorZahavich, LA-
dc.contributor.authorBeausejour-Ladouceur, V-
dc.contributor.authorJadhav, M-
dc.contributor.authorSkinner, JR-
dc.contributor.authorFranciosi, S-
dc.contributor.authorKrahn, AD-
dc.contributor.authorAbdelsayed, M-
dc.contributor.authorRuben, PC-
dc.contributor.authorYung, TC-
dc.contributor.authorAckerman, MJ-
dc.contributor.authorWilde, AA-
dc.contributor.authorSchwartz, PJ-
dc.contributor.authorProbst, V-
dc.date.accessioned2018-09-14T08:43:38Z-
dc.date.available2018-09-14T08:43:38Z-
dc.date.issued2018-
dc.identifier.citationEuropean Heart Journal, 2018, v. 39, p. 2879-2887-
dc.identifier.issn0195-668X-
dc.identifier.urihttp://hdl.handle.net/10722/260555-
dc.languageeng-
dc.relation.ispartofEuropean Heart Journal-
dc.subjectBrugada syndrome-
dc.subjectGenotype-phenotype correlation-
dc.subjectLong QT syndrome-
dc.subjectProgressive cardiac conduction disorders-
dc.subjectSCN5A-
dc.subjectSodium channelopathy-
dc.titleSCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups-
dc.typeArticle-
dc.identifier.emailKwok, SY: ksy464@hku.hk-
dc.identifier.emailYung, TC: tcyung@hkusua.hku.hk-
dc.identifier.doi10.1093/eurheartj/ehy412-
dc.identifier.scopuseid_2-s2.0-85055420900-
dc.identifier.hkuros290097-
dc.identifier.volume39-
dc.identifier.spage2879-
dc.identifier.epage2887-
dc.identifier.eissn1522-9645-
dc.identifier.isiWOS:000442981200009-
dc.identifier.issnl0195-668X-

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