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APA Citation
Ng, B. G., Lourenço, C. M., Losfeld, M., Buckingham, K. J., Kircher, M., Nickerson, D. A., Shendure, J., Bamshad, M. J., , , & Freeze, H. H. (2019). mutations in the translocon‐associated protein complex subunit SSR3 cause a novel congenital disorder of glycosylation. Journal of inherited metabolic disease, 42(5), 993–997. http://access.bl.uk/ark:/81055/vdc_100091287243.0x00004b