Cite
MLA Citation
Bobby G. Ng et al.. “Mutations in the translocon‐associated protein complex subunit SSR3 cause a novel congenital disorder of glycosylation.” Journal of inherited metabolic disease, vol. 42, no. 5, 2019, pp. 993–997. http://access.bl.uk/ark:/81055/vdc_100091287243.0x00004b