Chou, J., Hanna-Wakim, R., Tirosh, I., Kane, J., Fraulino, D., Lee, Y. N., . . . Massaad, M. J. (2012). A novel homozygous mutation in Recombination Activating Gene 2 in two relatives with different clinical phenotypes: Omenn syndrome and Hyper-IgM syndrome.
Citação norma ChicagoChou, Janet, et al. A Novel Homozygous Mutation in Recombination Activating Gene 2 in Two Relatives With Different Clinical Phenotypes: Omenn Syndrome and Hyper-IgM Syndrome. 2012.
Citação norma MLAChou, Janet, et al. A Novel Homozygous Mutation in Recombination Activating Gene 2 in Two Relatives With Different Clinical Phenotypes: Omenn Syndrome and Hyper-IgM Syndrome. 2012.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.