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 APA Style APA-ALL Style AAA 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., Michels, M., de Coo, R., Hoedemaekers, Y.& 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.https://doi.org/10.1038/ejhg.2014.211

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