Characterization of a disease-causing Lys329 to Glu mutation in 16 patients with medium-chain acyl-CoA dehydrogenase deficiency.

MLA

Gregersen, N., et al. “Characterization of a Disease-Causing Lys329 to Glu Mutation in 16 Patients with Medium-Chain Acyl-CoA Dehydrogenase Deficiency.” Journal of Inherited Metabolic Disease, vol. 14, no. 3, 1991, pp. 314–16. EBSCOhost, https://doi.org/10.1007/BF01811691.

APA

Gregersen, N., Andresen, B. S., Bross, P., Winter, V., Rüdiger, N., Engst, S., Ghisla, S., Christensen, E., Kelly, D., Strauss, A. W., & et. al. (1991). Characterization of a disease-causing Lys329 to Glu mutation in 16 patients with medium-chain acyl-CoA dehydrogenase deficiency. Journal of Inherited Metabolic Disease, 14(3), 314–316. https://doi.org/10.1007/BF01811691

Chicago

Gregersen, N, B S Andresen, P Bross, V Winter, N Rüdiger, S Engst, S Ghisla, et al. 1991. “Characterization of a Disease-Causing Lys329 to Glu Mutation in 16 Patients with Medium-Chain Acyl-CoA Dehydrogenase Deficiency.” Journal of Inherited Metabolic Disease 14 (3): 314–16. doi:10.1007/BF01811691.