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