Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy
Abstract. Hypertrophic cardiomyopathy (HCM) is characterized by asymmetric left ventricular hypertrophy, diastolic dysfunction and myocardial disarray. HCM is
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| Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
April 20, 2012
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| In: |
Human molecular genetics
Year: 2012, Jahrgang: 21, Heft: 14, Pages: 3237-3254 |
| ISSN: | 1460-2083 |
| DOI: | 10.1093/hmg/dds157 |
| Online-Zugang: | Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1093/hmg/dds157 Verlag, kostenfrei, Volltext: https://academic.oup.com/hmg/article/21/14/3237/2386297 
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| Verfasserangaben: | Felix W. Friedrich, Brendan R. Wilding, Silke Reischmann, Claudia Crocini, Patrick Lang, Philippe Charron, Oliver J. Müller, Meagan J. McGrath, Ingra Vollert, Arne Hansen, Wolfgang A. Linke, Christian Hengstenberg, Gisèle Bonne, Stellan Morner, Thomas Wichter, Hugo Madeira, Eloisa Arbustini, Thomas Eschenhagen, Christina A. Mitchell, Richard Isnard, Lucie Carrier |
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| 520 | |a Abstract. Hypertrophic cardiomyopathy (HCM) is characterized by asymmetric left ventricular hypertrophy, diastolic dysfunction and myocardial disarray. HCM is | ||
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