The p.Ala2430Val mutation in filamin C causes a "hypertrophic myofibrillar 
cardiomyopathy"

Schaenzer, Anne; Schumann, Elisabeth; Zengeler, Diana; Gulatz, Lisann; Maroli, Giovanni; Ahting, Uwe; Sprengel, Anke; Graef, Sabine; Hahn, Andreas; Jux, Christian; Acker, Till; Fuerst, Dieter O.; Rupp, Stefan; Schuld, Julia; van der Ven, Peter F. M.

doi:10.1007/s10974-021-09601-1

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The p.Ala2430Val mutation in filamin C causes a "hypertrophic myofibrillar cardiomyopathy"

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Maroli, Giovanni
Cardiac Development and Remodeling, Max Planck Institute for Heart and Lung Research, Max Planck Society;

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Schaenzer, A., Schumann, E., Zengeler, D., Gulatz, L., Maroli, G., Ahting, U., et al. (2020). The p.Ala2430Val mutation in filamin C causes a "hypertrophic myofibrillar cardiomyopathy". JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY. doi:10.1007/s10974-021-09601-1.

Cite as: https://hdl.handle.net/21.11116/0000-0008-4C76-F

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