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APA Citation
Sabry, S., Vuillaumier-Barrot, S., Mintet, E., Fasseu, M., Valayannopoulos, V., Héron, D., Dorison, N., Mignot, C., Seta, N., Chantret, I., Dupré, T., & Moore, S. (2016). a case of fatal Type I congenital disorders of glycosylation (CDG I) associated with low dehydrodolichol diphosphate synthase (DHDDS) activity. Orphanet journal of rare diseases, 11(1), 1–14. http://access.bl.uk/ark:/81055/vdc_100080471224.0x00008d