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

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

44 Citations (Web of Science)
Original languageEnglish
Pages (from-to)922-928
JournalEuropean Journal of Human Genetics
Issue number7
Publication statusPublished - Jul 2015

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