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Details on Person 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
| Class:Id | LiteratureReference:1015729 |
|---|---|
| _displayName | 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 |
| _timestamp | 2010-11-15 14:08:06 |
| author | [Person:514618] Wang, Y [Person:570864] Schachter, H [Person:422443] Marth, JD |
| created | [InstanceEdit:1015777] Jassal, B, 2010-11-15 |
| journal | Biochim Biophys Acta |
| pages | 301-11 |
| pubMedIdentifier | 12417412 |
| title | 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 |
| volume | 1573 |
| year | 2002 |
| (literatureReference) | [Reaction:975829] Addition of a GlcNAc on the alpha 1,4 branch by MGAT2 [Homo sapiens] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by 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 (1015729)
