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

Marja W. Wessels, Johanna C. Herkert, Ingrid M. Frohn-Mulder, Michiel Dalinghaus, Arthur van den Wijngaard, Ronald R. de Krijger, Michelle Michels, Irenaeus F. M. de Coo, Yvonne M. Hoedemaekers, Dennis Dooijes

Research output: Contribution to journalArticleAcademicpeer-review

5 Citations (Scopus)
Original languageEnglish
Pages (from-to)922-928
JournalEuropean Journal of Human Genetics
Volume23
Issue number7
DOIs
Publication statusPublished - Jul 2015

Cite this

Wessels, M. W., Herkert, J. C., Frohn-Mulder, I. M., Dalinghaus, M., van den Wijngaard, A., de Krijger, R. R., Michels, M., de Coo, I. F. M., Hoedemaekers, Y. M., & 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