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(V1208) |
The RBM20-p.P638L mutation is associated with dilated cardiomyopathy and sudden cardiac death in two German families |
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A. Gärtner-Rommel, G. M. Cheung, K. G. Pohl, U. Schulz, K. T. Laser, J. Gummert, H. Milting (Bad Oeynhausen) |
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Diskussion |
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(V1209) |
Different DCM phenotypes of patients harboring diverse RBM20 mutations can be modeled by patient-specific induced pluripotent stem cell-derived cardiomyocytes |
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K. Streckfuß-Bömeke, M. Tiburcy, A. Fomin, C. Fischer, A. Perrot, C. Özcelik, S. T. Sossalla, W. Linke, W.-H. Zimmermann, G. Hasenfuß, K. Guan (Göttingen, Bochum, Berlin, Northeim) |
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Diskussion |
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(V1210) |
Systematic molecular genetic analysis in patients with premature myocardial infarction frequently unmasks familial hypercholesterolemia |
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I. Braenne, M. Kleinecke, B. Reiz, E. Graf, T. Strom, T. Wieland, M. Fischer, C. Hengstenberg, T. Meitinger, J. Erdmann, H. Schunkert (Lübeck, Neuherberg, Regensburg, München) |
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Diskussion |
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(V1211) |
Elucidating the pathomechanism of human DCM-causing titin mutations |
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W. Linke, J. T. Hinson, S. Swist, J. Seidman, C. Seidman (Bochum; Boston, US) |
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Diskussion |
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(V1212) |
Genetics of Left Ventricular Noncompaction Cardiomyopathy |
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J. Haas, F. Zhu, C. Geier, R. Pribe-Wolferts, K. S. Frese, E. Kayvanpour, F. Sedaghat-Hamedani, S. Mester, B. Peil, J. Lorenzo Bermejo, J. Franke, A. Keller, Y. Liao, H. A. Katus, B. Meder (Heidelberg, Berlin, Saarbrücken; Hubei, CN) |
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Diskussion |
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(V1213) |
Atlas of the Clinical Genetics of Human Dilated Cardiomyopathy |
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J. Haas, K. S. Frese, B. Peil, A. Keller, R. Nietsch, E. Kayvanpour, B. Vogel, F. Sedaghat-Hamedani, X. Zhao, V. King, E. Wirsz, A. Waldenstrom, M. Bolognesi, R. Bellazzi, S. Mörner, J. Lorenzo Bermejo, P. Elliott, E. Arbustini, H. A. Katus, B. Meder (Heidelberg, Saarbrücken; Princeton, US; Umeå, SE; Milano, Pavia, IT; London, UK) |
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Diskussion |