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

Author:

Wang Yan,Schachter Harry,Marth Jamey D

Publisher

Elsevier BV

Subject

Molecular Biology,Biochemistry,Biophysics

Reference36 articles.

1. The “yellow brick road” to branched complex N-glycans;Schachter;Glycobiology,1991

2. Carbohydrate-deficient glycoprotein syndrome type II—an autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS);Charuk;Eur. J. Biochem.,1995

3. Carbohydrate deficient glycoprotein syndrome type II: a deficiency in Golgi localised N-acetylglucosaminyltransferase II;Jaeken;Arch. Dis. Child.,1994

4. Carbohydrate-deficient glycoprotein syndrome Type II: an autosomal recessive disease due to mutations in the N-acetylglucosaminyltransferase II gene;Jaeken,1996

5. Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development;Tan;Am. J. Hum. Genet.,1996

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