Corzo, D., Gibson, W., Johnson, K., Mitchell, G., LePage, G., Cox, G. F., . . . Steinberg, S. J. (2002). Contiguous Deletion of the X-Linked Adrenoleukodystrophy Gene (ABCD1) and DXS1357E: A Novel Neonatal Phenotype Similar to Peroxisomal Biogenesis Disorders. The American Society of Human Genetics.
Citação norma ChicagoCorzo, Deyanira, et al. Contiguous Deletion of the X-Linked Adrenoleukodystrophy Gene (ABCD1) and DXS1357E: A Novel Neonatal Phenotype Similar to Peroxisomal Biogenesis Disorders. The American Society of Human Genetics, 2002.
Citação norma MLACorzo, Deyanira, et al. Contiguous Deletion of the X-Linked Adrenoleukodystrophy Gene (ABCD1) and DXS1357E: A Novel Neonatal Phenotype Similar to Peroxisomal Biogenesis Disorders. The American Society of Human Genetics, 2002.