Blommaert, E., PĂ©anne, R., Cherepanova, N. A., Rymen, D., Staels, F., Jaeken, J., . . . Matthijs, G. (2019). Mutations in MAGT1 lead to a glycosylation disorder with a variable phenotype. Proceedings of the National Academy of Sciences of the United States of America, 116(20), 9865.
Chicago Style (17th ed.) CitationBlommaert, Eline, et al. "Mutations in MAGT1 Lead to a Glycosylation Disorder with a Variable Phenotype." Proceedings of the National Academy of Sciences of the United States of America 116, no. 20 (2019): 9865.
MLA (8th ed.) CitationBlommaert, Eline, et al. "Mutations in MAGT1 Lead to a Glycosylation Disorder with a Variable Phenotype." Proceedings of the National Academy of Sciences of the United States of America, vol. 116, no. 20, 2019, p. 9865.
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