Loss of Nexilin function leads to a recessive lethal fetal cardiomyopathy 
characterized by cardiomegaly and endocardial fibroelastosis

Johansson, Josefin; Frykholm, Carina; Ericson, Katharina; Kazamia, Kalliopi; Lindberg, Amanda; Mulaiese, Nancy; Falck, Geir; Gustafsson, Per-Erik; Lideus, Sarah; Gudmundsson, Sanna; Ameur, Adam; Bondeson, Marie-Louise; Wilbe, Maria

doi:10.1002/ajmg.a.62685

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Loss of Nexilin function leads to a recessive lethal fetal cardiomyopathy characterized by cardiomegaly and endocardial fibroelastosis

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Johansson, J., Frykholm, C., Ericson, K., Kazamia, K., Lindberg, A., Mulaiese, N., Falck, G., Gustafsson, P.-E., Lideus, S., Gudmundsson, S., Ameur, A., Bondeson, M.-L., & Wilbe, M. (2022). Loss of Nexilin function leads to a recessive lethal fetal cardiomyopathy characterized by cardiomegaly and endocardial fibroelastosis. American Journal of Medical Genetics Part A, 188(6), 1676-1687. doi:10.1002/ajmg.a.62685.

引用: https://hdl.handle.net/21.11116/0000-000F-2016-4

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