Smits, P., Saada, A., Wortmann, S. B., Heister, A. J., Brink, M., Pfundt, R., . . . van den Heuvel, L. P. (2011). Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy. European journal of human genetics, 19(4), . https://doi.org/10.1038/ejhg.2010.214
Chicago-Zitierstil (17. Ausg.)Smits, Paulien, et al. "Mutation in Mitochondrial Ribosomal Protein MRPS22 Leads to Cornelia De Lange-like Phenotype, Brain Abnormalities and Hypertrophic Cardiomyopathy." European Journal of Human Genetics 19, no. 4 (2011). https://doi.org/10.1038/ejhg.2010.214.
MLA-Zitierstil (9. Ausg.)Smits, Paulien, et al. "Mutation in Mitochondrial Ribosomal Protein MRPS22 Leads to Cornelia De Lange-like Phenotype, Brain Abnormalities and Hypertrophic Cardiomyopathy." European Journal of Human Genetics, vol. 19, no. 4, 2011, https://doi.org/10.1038/ejhg.2010.214.