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In the version of this article initially published, Federico Manevy’s name appeared with a middle initial in error. The name has been corrected in the HTML and PDF versions of the article.

Barc, J., Tadros, R., Glinge, C., Chiang, D., Jouni, M., Simonet, F., et al. (2022). Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility (Nature Genetics, (2022), 54, 3, (232-239), 10.1038/s41588-021-01007-6) [Altro] [10.1038/s41588-022-01079-y].

Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility (Nature Genetics, (2022), 54, 3, (232-239), 10.1038/s41588-021-01007-6)

Lia Crotti;
2022

Abstract

In the version of this article initially published, Federico Manevy’s name appeared with a middle initial in error. The name has been corrected in the HTML and PDF versions of the article.
Altro
Scientifica
Alleles; Disease Susceptibility; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Microtubule-Associated Proteins; Mutation; NAV1.5 Voltage-Gated Sodium Channel; Young Adult; Brugada Syndrome
English
2022
https://doi.org/10.1038/s41588-021-01007-6
https://doi.org/10.1038/s41588-022-01079-y
Barc, J., Tadros, R., Glinge, C., Chiang, D., Jouni, M., Simonet, F., et al. (2022). Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility (Nature Genetics, (2022), 54, 3, (232-239), 10.1038/s41588-021-01007-6) [Altro] [10.1038/s41588-022-01079-y].
Barc, J; Tadros, R; Glinge, C; Chiang, D; Jouni, M; Simonet, F; Jurgens, S; Baudic, M; Nicastro, M; Potet, F; Offerhaus, J; Walsh, R; Hoan Choi, S; Verkerk, A; Mizusawa, Y; Anys, S; Minois, D; Arnaud, M; Duchateau, J; Wijeyeratne, Y; Muir, A; Papadakis, M; Castelletti, S; Torchio, M; Gil Ortuño, C; Lacunza, J; Giachino, D; Cerrato, N; Martins, R; Campuzano, O; Van Dooren, S; Thollet, A; Kyndt, F; Mazzanti, A; Clémenty, N; Bisson, A; Corveleyn, A; Stallmeyer, B; Dittmann, S; Saenen, J; Noël, A; Honarbakhsh, S; Rudic, B; Marzak, H; Rowe, M; Federspiel, C; Le Page, S; Placide, L; Milhem, A; Barajas-Martinez, H; Beckmann, B; Krapels, I; Steinfurt, J; Gregers Winkel, B; Jabbari, R; Shoemaker, M; Boukens, B; Škorić-Milosavljević, D; Bikker, H; Manevy, F; Lichtner, P; Ribasés, M; Meitinger, T; Müller-Nurasyid, M; Group, K; Veldink, J; van den Berg, L; Van Damme, P; Cusi, D; Lanzani, C; Rigade, S; Charpentier, E; Baron, E; Bonnaud, S; Lecointe, S; Donnart, A; Le Marec, H; Chatel, S; Karakachoff, M; Bézieau, S; London, B; Tfelt-Hansen, J; Roden, D; Odening, K; Cerrone, M; Chinitz, L; Volders, P; van de Berg, M; Laurent, G; Faivre, L; Antzelevitch, C; Kääb, S; Al Arnaout, A; Dupuis, J; Pasquie, J; Billon, O; Roberts, J; Jesel, L; Borggrefe, M; Lambiase, P; Mansourati, J; Loeys, B; Leenhardt, A; Guicheney, P; Maury, P; Schulze-Bahr, E; Robyns, T; Breckpot, J; Babuty, D; Priori, S; Napolitano, C; Referral Center for inherited cardiac arrhythmia, N; de Asmundis, C; Brugada, P; Brugada, R; Arbelo, E; Brugada, J; Mabo, P; Behar, N; Giustetto, C; Sabater Molina, M; Gimeno, J; Hasdemir, C; Schwartz, P; Crotti, L; Mckeown, P; Sharma, S; Behr, E; Haissaguerre, M; Sacher, F; Rooryck, C; Tan, H; Remme, C; Postema, P; Delmar, M; Ellinor, P; Lubitz, S; Gourraud, J; Tanck, M; L. George Jr., A; Macrae, C; Burridge, P; Dina, C; Probst, V; Wilde, A; Schott, J; Redon &, R; Bezzina, C
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/393715
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