Wessels, M. W., Herkert, J. C., Frohn-Mulder, I. M., Dalinghaus, M., van den Wijngaard, A., de Krijger, R. R., . . . Dooijes, D. (2015). Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects. Eur J Hum Genet.
Style de citation ChicagoWessels, Marja W., et al. "Compound Heterozygous or Homozygous Truncating MYBPC3 Mutations Cause Lethal Cardiomyopathy With Features of Noncompaction and Septal Defects." Eur J Hum Genet 2015.
Style de citation MLAWessels, Marja W., et al. "Compound Heterozygous or Homozygous Truncating MYBPC3 Mutations Cause Lethal Cardiomyopathy With Features of Noncompaction and Septal Defects." Eur J Hum Genet 2015.
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