APA (7th ed.) Citation

Dörre, K., Olczak, M., Wada, Y., Sosicka, P., Grüneberg, M., Reunert, J., . . . Marquardt, T. (2015). A new case of UDP-galactose transporter deficiency (SLC35A2-CDG): Molecular basis, clinical phenotype, and therapeutic approach. Journal of inherited metabolic disease, 38(5), 931-940. https://doi.org/10.1007/s10545-015-9828-6

Chicago Style (17th ed.) Citation

Dörre, K., et al. "A New Case of UDP-galactose Transporter Deficiency (SLC35A2-CDG): Molecular Basis, Clinical Phenotype, and Therapeutic Approach." Journal of Inherited Metabolic Disease 38, no. 5 (2015): 931-940. https://doi.org/10.1007/s10545-015-9828-6.

MLA (9th ed.) Citation

Dörre, K., et al. "A New Case of UDP-galactose Transporter Deficiency (SLC35A2-CDG): Molecular Basis, Clinical Phenotype, and Therapeutic Approach." Journal of Inherited Metabolic Disease, vol. 38, no. 5, 2015, pp. 931-940, https://doi.org/10.1007/s10545-015-9828-6.