Al-Hassnan, Z. N., Shinwari, Z. M., Wakil, S. M., Tulbah, S., Mohammed, S., Rahbeeni, Z., . . . Alburaiki, J. (2016). A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy. BMC Med Genet.
Citação norma ChicagoAl-Hassnan, Zuhair N., et al. "A Substitution Mutation in Cardiac Ubiquitin Ligase, FBXO32, Is Associated With an Autosomal Recessive Form of Dilated Cardiomyopathy." BMC Med Genet 2016.
Citação norma MLAAl-Hassnan, Zuhair N., et al. "A Substitution Mutation in Cardiac Ubiquitin Ligase, FBXO32, Is Associated With an Autosomal Recessive Form of Dilated Cardiomyopathy." BMC Med Genet 2016.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.