APA (7th ed.) Citation

Kožich, V., Sokolová, J., Morris, A. A. M., Pavlíková, M., Gleich, F., Kölker, S., . . . Huemer, M. (2021). Cystathionine β-synthase deficiency in the E-HOD registry-part I: Pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis. Journal of inherited metabolic disease, 44(3), . https://doi.org/10.1002/jimd.12338

Chicago Style (17th ed.) Citation

Kožich, Viktor, et al. "Cystathionine β-synthase Deficiency in the E-HOD Registry-part I: Pyridoxine Responsiveness as a Determinant of Biochemical and Clinical Phenotype at Diagnosis." Journal of Inherited Metabolic Disease 44, no. 3 (2021). https://doi.org/10.1002/jimd.12338.

MLA (9th ed.) Citation

Kožich, Viktor, et al. "Cystathionine β-synthase Deficiency in the E-HOD Registry-part I: Pyridoxine Responsiveness as a Determinant of Biochemical and Clinical Phenotype at Diagnosis." Journal of Inherited Metabolic Disease, vol. 44, no. 3, 2021, https://doi.org/10.1002/jimd.12338.