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

author
created [InstanceEdit:1015777] Jassal, B, 2010-11-15
dbId 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
journal Biochim Biophys Acta
pages 301-11
pubMedIdentifier 12417412
schemaClass LiteratureReference
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
url http://www.ncbi.nlm.nih.gov/pubmed/12417412
volume 1573
year 2002
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