Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disea...
Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
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Author / Creator
Bezzina, Connie R , Barc, Julien , Mizusawa, Yuka , Remme, Carol Ann , Gourraud, Jean-Baptiste , Simonet, Floriane , Verkerk, Arie O , Schwartz, Peter J , Crotti, Lia , Dagradi, Federica , Guicheney, Pascale , Fressart, Véronique , Leenhardt, Antoine , Antzelevitch, Charles , Bartkowiak, Susan , Schulze-Bahr, Eric , Zumhagen, Sven , Behr, Elijah R , Bastiaenen, Rachel , Tfelt-Hansen, Jacob , Olesen, Morten Salling , Kääb, Stefan , Beckmann, Britt M , Weeke, Peter , Watanabe, Hiroshi , Endo, Naoto , Minamino, Tohru , Horie, Minoru , Ohno, Seiko , Hasegawa, Kanae , Makita, Naomasa , Nogami, Akihiko , Shimizu, Wataru , Aiba, Takeshi , Froguel, Philippe , Balkau, Beverley , Lantieri, Olivier , Torchio, Margherita , Wiese, Cornelia , Weber, David , Wolswinkel, Rianne , Coronel, Ruben , Boukens, Bas J , Bézieau, Stéphane , Charpentier, Eric , Chatel, Stéphanie , Despres, Aurore , Gros, Françoise , Kyndt, Florence , Lecointe, Simon , Lindenbaum, Pierre , Portero, Vincent , Violleau, Jade , Gessler, Manfred , Tan, Hanno L , Roden, Dan M , Christoffels, Vincent M , Le Marec, Hervé , Wilde, Arthur A , Probst, Vincent , Schott, Jean-Jacques , Dina, Christian and Redon, Richard
Publisher
New York: Nature Publishing Group US
Journal title
Language
English
Formats
Publication information
Publisher
New York: Nature Publishing Group US
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More information
Scope and Contents
Contents
Nat. Genet. 45, 1044–1049 (2013); published online 21 July 2013; corrected after print 4 October 2013 In the version of this article initially published, Martin Borggrefe and Rainer Schimpf were inadvertently omitted from the author list. Both are affiliated with the First Department of Medicine (Cardiology), University Medical Center, Medical Facu...
Alternative Titles
Full title
Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
Authors, Artists and Contributors
Author / Creator
Barc, Julien
Mizusawa, Yuka
Remme, Carol Ann
Gourraud, Jean-Baptiste
Simonet, Floriane
Verkerk, Arie O
Schwartz, Peter J
Crotti, Lia
Dagradi, Federica
Guicheney, Pascale
Fressart, Véronique
Leenhardt, Antoine
Antzelevitch, Charles
Bartkowiak, Susan
Schulze-Bahr, Eric
Zumhagen, Sven
Behr, Elijah R
Bastiaenen, Rachel
Tfelt-Hansen, Jacob
Olesen, Morten Salling
Kääb, Stefan
Beckmann, Britt M
Weeke, Peter
Watanabe, Hiroshi
Endo, Naoto
Minamino, Tohru
Horie, Minoru
Ohno, Seiko
Hasegawa, Kanae
Makita, Naomasa
Nogami, Akihiko
Shimizu, Wataru
Aiba, Takeshi
Froguel, Philippe
Balkau, Beverley
Lantieri, Olivier
Torchio, Margherita
Wiese, Cornelia
Weber, David
Wolswinkel, Rianne
Coronel, Ruben
Boukens, Bas J
Bézieau, Stéphane
Charpentier, Eric
Chatel, Stéphanie
Despres, Aurore
Gros, Françoise
Kyndt, Florence
Lecointe, Simon
Lindenbaum, Pierre
Portero, Vincent
Violleau, Jade
Gessler, Manfred
Tan, Hanno L
Roden, Dan M
Christoffels, Vincent M
Le Marec, Hervé
Wilde, Arthur A
Probst, Vincent
Schott, Jean-Jacques
Dina, Christian
Redon, Richard
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_crossref_citationtrail_10_1038_ng1113_1409b
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_crossref_citationtrail_10_1038_ng1113_1409b
Other Identifiers
ISSN
1061-4036
E-ISSN
1546-1718
DOI
10.1038/ng1113-1409b
