MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If
J. Clin. Invest. Barbara Schenk, et al. 108:1687 doi:10.1172/JCI13419 [Go to this article.]

Table 2
Complementation of the deficiency in LLO biosynthesis in patient fibroblast by expression of Lec35 cDNA