Huemer, M., & Trefz, F. K. (2016). Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency. Journal of inherited metabolic disease, 39(1), . https://doi.org/10.1007/s10545-015-9860-6
Chicago Style (17th ed.) CitationHuemer, Martina, and Friedrich K. Trefz. "Clinical Pattern, Mutations and in Vitro Residual Activity in 33 Patients with Severe 5, 10 Methylenetetrahydrofolate Reductase (MTHFR) Deficiency." Journal of Inherited Metabolic Disease 39, no. 1 (2016). https://doi.org/10.1007/s10545-015-9860-6.
MLA (9th ed.) CitationHuemer, Martina, and Friedrich K. Trefz. "Clinical Pattern, Mutations and in Vitro Residual Activity in 33 Patients with Severe 5, 10 Methylenetetrahydrofolate Reductase (MTHFR) Deficiency." Journal of Inherited Metabolic Disease, vol. 39, no. 1, 2016, https://doi.org/10.1007/s10545-015-9860-6.