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

Marja Wessels; JC Herkert; Ingrid Mulder; M. Dalinghaus; A van den Wijngaard; Ronald de Krijger; Michelle Michels; IFM Coo; YM Hoedemaekers; D 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 Wessels, JC Herkert, Ingrid Mulder, M. Dalinghaus, A van den Wijngaard, Ronald de Krijger, Michelle Michels, IFM Coo, YM Hoedemaekers, D Dooijes

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

67 Citations (Scopus)

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

Research programs

EMC COEUR-09
EMC MGC-02-96-01
EMC MM-03-24-01
EMC MM-04-44-02

Access to Document

10.1038/ejhg.2014.211

Cite this

Wessels, M., Herkert, JC., Mulder, I., Dalinghaus, M., van den Wijngaard, A., de Krijger, R., Michels, M., 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, 23(7), 922-928. https://doi.org/10.1038/ejhg.2014.211

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author = "Marja Wessels and JC Herkert and Ingrid Mulder and M. Dalinghaus and {van den Wijngaard}, A and {de Krijger}, Ronald and Michelle Michels and IFM Coo and YM Hoedemaekers and D Dooijes",

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Wessels, M, Herkert, JC, Mulder, I, Dalinghaus, M, van den Wijngaard, A, de Krijger, R , Michels, M, 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

TY - JOUR

T1 - Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects

AU - Wessels, Marja

AU - Herkert, JC

AU - Mulder, Ingrid

AU - Dalinghaus, M.

AU - van den Wijngaard, A

AU - de Krijger, Ronald

AU - Michels, Michelle

AU - Coo, IFM

AU - Hoedemaekers, YM

AU - Dooijes, D

PY - 2015

Y1 - 2015

U2 - 10.1038/ejhg.2014.211

DO - 10.1038/ejhg.2014.211

M3 - Article

C2 - 25335496

SN - 1018-4813

VL - 23

SP - 922

EP - 928

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 7

ER -