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2001 | 1 |
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Mice with a homozygous deletion of the Mgat2 gene encoding UDP-N-acetylglucosamine:alpha-6-D-mannoside beta1,2-N-acetylglucosaminyltransferase II: a model for congenital disorder of glycosylation type IIa.
Biochim Biophys Acta. 2002 Dec 19;1573(3):301-11. doi: 10.1016/s0304-4165(02)00397-5.
Biochim Biophys Acta. 2002.
PMID: 12417412
Review.
Modeling human congenital disorder of glycosylation type IIa in the mouse: conservation of asparagine-linked glycan-dependent functions in mammalian physiology and insights into disease pathogenesis.
Wang Y, Tan J, Sutton-Smith M, Ditto D, Panico M, Campbell RM, Varki NM, Long JM, Jaeken J, Levinson SR, Wynshaw-Boris A, Morris HR, Le D, Dell A, Schachter H, Marth JD.
Wang Y, et al.
Glycobiology. 2001 Dec;11(12):1051-70. doi: 10.1093/glycob/11.12.1051.
Glycobiology. 2001.
PMID: 11805078
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