Double heterozygous mutation of KCNH2 and ANK2 leads to phenotypical 
aggravation of congenital long QT syndrome

Schweizer, Patrick; Runge, Sarah; Gessner, Guido; Heinemann, Stefan H.; Zehelein, Joerg; Koenen, Michael; Khalil, Markus; Ulmer, Herbert E.; Koenen, Michael; Katus, Hugo A.; Becker, Rüdiger; Thomas, Dierck

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Double heterozygous mutation of KCNH2 and ANK2 leads to phenotypical aggravation of congenital long QT syndrome

Schweizer, P., Runge, S., Gessner, G., Heinemann, S. H., Zehelein, J., Koenen, M., et al. (2010). Double heterozygous mutation of KCNH2 and ANK2 leads to phenotypical aggravation of congenital long QT syndrome. Poster presented at Heart Rhythm 2010.

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Datensatz-Permalink: https://hdl.handle.net/11858/00-001M-0000-002E-8018-8 Versions-Permalink: https://hdl.handle.net/11858/00-001M-0000-002E-8019-6

Genre: Poster

Alternativer Titel : Double heterozygous mutation of KCNH2 and ANK2 leads to phenotypical aggravation of congenital long QT syndrome

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Urheber:
Schweizer, Patrick^{1, 2}, Autor
Runge, Sarah, Autor
Gessner, Guido, Autor
Heinemann, Stefan H., Autor
Zehelein, Joerg², Autor
Koenen, Michael^{1, 2}, Autor
Khalil, Markus, Autor
Ulmer, Herbert E., Autor
Koenen, Michael^{1, 2}, Autor
Katus, Hugo A., Autor
Becker, Rüdiger, Autor
Thomas, Dierck, Autor

Affiliations:
1Department of Cell Physiology, Max Planck Institute for Medical Research, Max Planck Society, ou_1497701
2Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Max Planck Society, ou_1497704