Corrigendum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
Both are affiliated with the First Department of Medicine (Cardiology), University Medical Center, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany, and with DZHK (German Centre for Cardiovascular Research), partner site Heidelberg/Mannheim, Mannheim, Germany.
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| Veröffentlicht in: | Nature genetics 2013-11, Vol.45 (11), p.1409 |
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| 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 Redon, Richard |
| description | Both are affiliated with the First Department of Medicine (Cardiology), University Medical Center, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany, and with DZHK (German Centre for Cardiovascular Research), partner site Heidelberg/Mannheim, Mannheim, Germany. |
| format | Article |
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Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><jtitle>Nature genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bezzina, Connie R</au><au>Barc, Julien</au><au>Mizusawa, Yuka</au><au>Remme, Carol Ann</au><au>Gourraud, Jean-Baptiste</au><au>Simonet, Floriane</au><au>Verkerk, Arie O</au><au>Schwartz, Peter J</au><au>Crotti, Lia</au><au>Dagradi, Federica</au><au>Guicheney, Pascale</au><au>Fressart, Véronique</au><au>Leenhardt, Antoine</au><au>Antzelevitch, Charles</au><au>Bartkowiak, Susan</au><au>Schulze-Bahr, Eric</au><au>Zumhagen, Sven</au><au>Behr, Elijah R</au><au>Bastiaenen, Rachel</au><au>Tfelt-Hansen, Jacob</au><au>Olesen, Morten Salling</au><au>Kääb, Stefan</au><au>Beckmann, Britt M</au><au>Weeke, Peter</au><au>Watanabe, Hiroshi</au><au>Endo, Naoto</au><au>Minamino, Tohru</au><au>Horie, Minoru</au><au>Ohno, Seiko</au><au>Hasegawa, Kanae</au><au>Makita, Naomasa</au><au>Nogami, Akihiko</au><au>Shimizu, Wataru</au><au>Aiba, Takeshi</au><au>Froguel, Philippe</au><au>Balkau, Beverley</au><au>Lantieri, Olivier</au><au>Torchio, Margherita</au><au>Wiese, Cornelia</au><au>Weber, David</au><au>Wolswinkel, Rianne</au><au>Coronel, Ruben</au><au>Boukens, Bas J</au><au>Bézieau, Stéphane</au><au>Charpentier, Eric</au><au>Chatel, Stéphanie</au><au>Despres, Aurore</au><au>Gros, Françoise</au><au>Kyndt, Florence</au><au>Lecointe, Simon</au><au>Lindenbaum, Pierre</au><au>Portero, Vincent</au><au>Violleau, Jade</au><au>Gessler, Manfred</au><au>Tan, Hanno L</au><au>Roden, Dan M</au><au>Christoffels, Vincent M</au><au>Le Marec, Hervé</au><au>Wilde, Arthur A</au><au>Probst, Vincent</au><au>Schott, Jean-Jacques</au><au>Dina, Christian</au><au>Redon, Richard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Corrigendum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death</atitle><jtitle>Nature genetics</jtitle><date>2013-11-01</date><risdate>2013</risdate><volume>45</volume><issue>11</issue><spage>1409</spage><pages>1409-</pages><issn>1061-4036</issn><eissn>1546-1718</eissn><abstract>Both are affiliated with the First Department of Medicine (Cardiology), University Medical Center, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany, and with DZHK (German Centre for Cardiovascular Research), partner site Heidelberg/Mannheim, Mannheim, Germany.</abstract><cop>New York</cop><pub>Nature Publishing Group</pub><tpages>1</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1061-4036 |
| ispartof | Nature genetics, 2013-11, Vol.45 (11), p.1409 |
| issn | 1061-4036 1546-1718 |
| language | eng |
| recordid | cdi_proquest_journals_1467256713 |
| source | Springer Journals; Springer Nature - Connect here FIRST to enable access |
| subjects | Defibrillators Heart attacks |
| title | Corrigendum: 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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