Kuilenburg, A. v., Dobritzsch, D., Meijer, J., Meinsma, R., Benoist, J., Assmann, B., . . . Hennekam, R. C. M. (2010). Dihydropyrimidinase deficiency: Phenotype, genotype and structural consequences in 17 patients. Biochimica et biophysica acta. Molecular basis of disease, 1802(7/8), . https://doi.org/10.1016/j.bbadis.2010.03.013
Chicago Style (17th ed.) CitationKuilenburg, André van, et al. "Dihydropyrimidinase Deficiency: Phenotype, Genotype and Structural Consequences in 17 Patients." Biochimica Et Biophysica Acta. Molecular Basis of Disease 1802, no. 7/8 (2010). https://doi.org/10.1016/j.bbadis.2010.03.013.
MLA (9th ed.) CitationKuilenburg, André van, et al. "Dihydropyrimidinase Deficiency: Phenotype, Genotype and Structural Consequences in 17 Patients." Biochimica Et Biophysica Acta. Molecular Basis of Disease, vol. 1802, no. 7/8, 2010, https://doi.org/10.1016/j.bbadis.2010.03.013.