Tuwaijri, A. A., Alyafee, Y., Umair, M., Alsubait, A., Alharbi, M., AlEidi, H., . . . Alfadhel, M. (2023). Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype. Wiley.
Citace podle Chicago (17th ed.)Tuwaijri, Abeer Al, et al. Congenital Disorder of Glycosylation with Defective Fucosylation 2 (FCSK Gene Defect): The Third Report in the Literature with a Mild Phenotype. Wiley, 2023.
Citace podle MLA (9th ed.)Tuwaijri, Abeer Al, et al. Congenital Disorder of Glycosylation with Defective Fucosylation 2 (FCSK Gene Defect): The Third Report in the Literature with a Mild Phenotype. Wiley, 2023.
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