Cite
HARVARD Citation
Ng, B. et al. (2019). Mutations in the translocon‐associated protein complex subunit SSR3 cause a novel congenital disorder of glycosylation. Journal of inherited metabolic disease. 42 (5), pp. 993-997. [Online].
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Ng, B. et al. (2019). Mutations in the translocon‐associated protein complex subunit SSR3 cause a novel congenital disorder of glycosylation. Journal of inherited metabolic disease. 42 (5), pp. 993-997. [Online].