Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik

Human Molecular Genetics - Tập 13 Số 5 - Trang 535-542
Claudia E. Grubenmann1
1Institute of Physiology, University of Zu¨rich, Winterthurerstrasse 190, 8057 Zu¨rich, Switzerland

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