Friedrich, Felix W. 
; Wilding, Brendan R. ; Reischmann, Silke ; Crocini, Claudia ; Lang, Patrick ; Charron, Philippe ; Müller, Oliver J. ; McGrath, Meagan J. ; Vollert, Ingra ; Hansen, Arne ; Linke, Wolfgang A. ; Hengstenberg, Christian ; Bonne, Gisèle ; Morner, Stellan ; Wichter, Thomas ; Madeira, Hugo ; Arbustini, Eloisa ; Eschenhagen, Thomas ; Mitchell, Christina A. ; Isnard, Richard ; Carrier, Lucie
; Wilding, Brendan R. ; Reischmann, Silke ; Crocini, Claudia ; Lang, Patrick ; Charron, Philippe ; Müller, Oliver J. ; McGrath, Meagan J. ; Vollert, Ingra ; Hansen, Arne ; Linke, Wolfgang A. ; Hengstenberg, Christian ; Bonne, Gisèle ; Morner, Stellan ; Wichter, Thomas ; Madeira, Hugo ; Arbustini, Eloisa ; Eschenhagen, Thomas ; Mitchell, Christina A. ; Isnard, Richard ; Carrier, Lucie 
Zusammenfassung
Hypertrophic cardiomyopathy (HCM) is characterized by asymmetric left ventricular hypertrophy, diastolic dysfunction and myocardial disarray. HCM is caused by mutations in sarcomeric genes, but in 40 of patients, the mutation is not yet identified. We hypothesized that FHL1, encoding four-and-a-half-LIM domains 1, could be another disease gene since it has been shown to cause distinct myopathies, ...
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