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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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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-002E-8018-8 Version Permalink: http://hdl.handle.net/11858/00-001M-0000-002E-8019-6
Genre: Poster
Alternative Title : Double heterozygous mutation of KCNH2 and ANK2 leads to phenotypical aggravation of congenital long QT syndrome

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 Creators:
Schweizer, Patrick1, 2, Author              
Runge, Sarah, Author
Gessner, Guido, Author
Heinemann, Stefan H., Author
Zehelein, Joerg2, Author              
Koenen, Michael1, 2, Author              
Khalil, Markus, Author
Ulmer, Herbert E., Author
Koenen, Michael1, 2, Author              
Katus, Hugo A., Author
Becker, Rüdiger, Author
Thomas, Dierck, Author
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              

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Language(s): eng - English
 Dates: 201020102010-05-12
 Publication Status: Published in print
 Pages: 1
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 664592
Other: 7571
 Degree: -

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Title: Heart Rhythm 2010
Place of Event: -
Start-/End Date: 2010-05 - 2010-05

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