Homozygous Truncating Variant in PKP2 Causes Hypoplastic Left Heart Syndrome

2018-12-01

Circulation. Genomic and precision medicine , Volume 11 - Issue 12 p. e002397

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Keywords	family, genetic testing, heart defects, congenital, hypoplastic left heart syndrome, mutation, myocardium, plakophilin
Persistent URL	doi.org/10.1161/CIRCGEN.118.002397, hdl.handle.net/1765/113487
Journal	Circulation. Genomic and precision medicine
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	Verhagen, J., van den Born, M., Kurul, S. (Serife), Asimaki, A. (Angeliki), van de Laar, I., Frohn-Mulder, I., … Wessels, M. (2018). Homozygous Truncating Variant in PKP2 Causes Hypoplastic Left Heart Syndrome. Circulation. Genomic and precision medicine, 11(12). doi:10.1161/CIRCGEN.118.002397

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