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Mice with a homozygous deletion of the Mgat2 gene encoding UDP-N-acetylglucosamine:α-6-d-mannoside β1,2-N-acetylglucosaminyltransferase II: a model for congenital disorder of glycosylation type IIa

✍ Scribed by Yan Wang; Harry Schachter; Jamey D Marth

Book ID: 117481052
Publisher: Elsevier Science
Year: 2002
Tongue: English
Weight: 496 KB
Volume: 1573
Category: Article
ISSN: 0304-4165
DOI: 10.1016/s0304-4165(02)00397-5

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