Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects

2015

European Journal of Human Genetics , Volume 23 - Issue 7 p. 922- 928

Additional Metadata
Persistent URL	doi.org/10.1038/ejhg.2014.211, hdl.handle.net/1765/85935
Journal	European Journal of Human Genetics
Organisation	Department of Cardiology
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Wessels, M., Herkert, J., Frohn-Mulder, I., Dalinghaus, M., van den Wijngaard, A., de Krijger, R., … Dooijes, D. (2015). Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects. European Journal of Human Genetics, 23(7), 922–928. doi:10.1038/ejhg.2014.211

Publication