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APA Citation
Dörre, K., Olczak, M., Wada, Y., Sosicka, P., Grüneberg, M., Reunert, J., Kurlemann, G., Fiedler, B., Biskup, S., Hörtnagel, K., Rust, S., & 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. http://access.bl.uk/ark:/81055/vdc_100079077223.0x00003f