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

doi:10.1038/ejhg.2014.211

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

Original language	English
Pages (from-to)	922-928
Journal	European Journal of Human Genetics
Volume	23
Issue number	7
DOIs	https://doi.org/10.1038/ejhg.2014.211
Publication status	Published - Jul 2015

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10.1038/ejhg.2014.211

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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

Wessels, Marja W. ; Herkert, Johanna C. ; Frohn-Mulder, Ingrid M. ; Dalinghaus, Michiel ; van den Wijngaard, Arthur ; de Krijger, Ronald R. ; Michels, Michelle ; de Coo, Irenaeus F. M. ; Hoedemaekers, Yvonne M. ; Dooijes, Dennis. / Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects. In: European Journal of Human Genetics. 2015 ; Vol. 23, No. 7. pp. 922-928.

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

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

year = "2015",

month = jul,

doi = "10.1038/ejhg.2014.211",

language = "English",

volume = "23",

pages = "922--928",

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Wessels, MW, Herkert, JC, Frohn-Mulder, IM, Dalinghaus, M, van den Wijngaard, A, de Krijger, RR, Michels, M, de Coo, IFM, Hoedemaekers, YM & 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, vol. 23, no. 7, pp. 922-928. https://doi.org/10.1038/ejhg.2014.211

Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects. / Wessels, Marja W.; Herkert, Johanna C.; Frohn-Mulder, Ingrid M.; Dalinghaus, Michiel; van den Wijngaard, Arthur; de Krijger, Ronald R.; Michels, Michelle; de Coo, Irenaeus F. M.; Hoedemaekers, Yvonne M.; Dooijes, Dennis.

In: European Journal of Human Genetics, Vol. 23, No. 7, 07.2015, p. 922-928.

Research output: Contribution to journal › Article › Academic › peer-review

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AU - Wessels, Marja W.

AU - Herkert, Johanna C.

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AU - Dalinghaus, Michiel

AU - van den Wijngaard, Arthur

AU - de Krijger, Ronald R.

AU - Michels, Michelle

AU - de Coo, Irenaeus F. M.

AU - Hoedemaekers, Yvonne M.

AU - Dooijes, Dennis

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JO - European Journal of Human Genetics

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SN - 1018-4813

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