Anzahl der Einträge: 1.
Artikel
Garnier, Sophie ![ORCID 0000-0002-7492-1617](/images/orcid_16x16.gif)
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Harakalova, Magdalena,
Weiss, Stefan ![ORCID 0000-0002-3553-4315](/images/orcid_16x16.gif)
,
Mokry, Michal,
Regitz-Zagrosek, Vera ![ORCID 0000-0002-3566-3467](/images/orcid_16x16.gif)
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Hengstenberg, Christian,
Cappola, Thomas P.,
Isnard, Richard,
Arbustini, Eloisa ![ORCID 0000-0003-2948-7994](/images/orcid_16x16.gif)
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Cook, Stuart A.,
van Setten, Jessica,
Calis, Jorg J. A.,
Hakonarson, Hakon,
Morley, Michael P.,
Stark, Klaus,
Prasad, Sanjay K.,
Li, Jin,
O'Regan, Declan P. ![ORCID 0000-0002-0691-0270](/images/orcid_16x16.gif)
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Grasso, Maurizia,
Müller-Nurasyid, Martina,
Meitinger, Thomas,
Empana, Jean-Philippe,
Strauch, Konstantin,
Waldenberger, Melanie,
Marguiles, Kenneth B.,
Seidman, Christine E.,
Kararigas, Georgios ![ORCID 0000-0002-8187-0176](/images/orcid_16x16.gif)
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Meder, Benjamin,
Haas, Jan,
Boutouyrie, Pierre,
Lacolley, Patrick,
Jouven, Xavier,
Erdmann, Jeanette ![ORCID 0000-0002-4486-6231](/images/orcid_16x16.gif)
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Blankenberg, Stefan,
Wichter, Thomas,
Ruppert, Volker,
Tavazzi, Luigi,
Dubourg, Olivier,
Roizes, Gérard,
Dorent, Richard,
de Groote, Pascal,
Fauchier, Laurent,
Trochu, Jean-Noël,
Aupetit, Jean-François,
Bilinska, Zofia T.,
Germain, Marine,
Völker, Uwe,
Hemerich, Daiane,
Raji, Ibticem,
Bacq-Daian, Delphine,
Proust, Carole,
Remior, Paloma,
Gomez-Bueno, Manuel ![ORCID 0000-0002-9764-7518](/images/orcid_16x16.gif)
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Lehnert, Kristin,
Maas, Renee,
Olaso, Robert,
Saripella, Ganapathi Varma,
Felix, Stephan B.,
McGinn, Steven,
Duboscq-Bidot, Laëtitia,
van Mil, Alain ![ORCID 0000-0001-9906-5047](/images/orcid_16x16.gif)
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Besse, Céline,
Fontaine, Vincent,
Blanché, Hélène,
Ader, Flavie,
Keating, Brendan,
Curjol, Angélique,
Boland, Anne,
Komajda, Michel,
Cambien, François,
Deleuze, Jean-Francois,
Dörr, Marcus,
Asselbergs, Folkert W. ![ORCID 0000-0002-1692-8669](/images/orcid_16x16.gif)
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Villard, Eric,
Trégouët, David-Alexandre und
Charron, Philippe
(2021)
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.
European Heart Journal 42 (20), S. 2000-2011.
Volltext nicht vorhanden.
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