Original language | English |
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Pages (from-to) | 922-928 |
Journal | European Journal of Human Genetics |
Volume | 23 |
Issue number | 7 |
DOIs | |
Publication status | Published - Jul 2015 |
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 journal › Article › Academic › peer-review
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