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Deficiency of UDP galactose:N acetylglucosamine β 1,4 galactosyltransferase I causes the congenital disorder of glycosylation type IId

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Figure

Figure 1
Figure 3Determination of UDP-[
Figure 5
Figure 6Localization of wild-type and 1031-1032insC β4GalT I overexpressed in COS-7 cells
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