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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 JH, Tan J, Bernardini M, Haddad S, Reithmeier RA, Jaeken J, Schachter H. Charuk JH, et al. Eur J Biochem. 1995 Jun 1;230(2):797-805. doi: 10.1111/j.1432-1033.1995.0797h.x. Eur J Biochem. 1995. PMID: 7607254 Free article.
Identification of P-glycoprotein in renal brush border membranes.
Lieberman DM, Reithmeier RA, Ling V, Charuk JH, Goldberg H, Skorecki KL. Lieberman DM, et al. Among authors: charuk jh. Biochem Biophys Res Commun. 1989 Jul 14;162(1):244-52. doi: 10.1016/0006-291x(89)91988-8. Biochem Biophys Res Commun. 1989. PMID: 2568833
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