ALG6/YOR002W Literature Guide Help

Other names published for ALG6: dolichyl-P-Glc:Man(9)GlcNAc(2)-PP-dolichol alpha-1,3-glucosyltransferase, YOR002W

ALG6 - Disease Gene Related (4)

ReferenceOther Genes Addressed
Imbach T, et al.  (2000) Multi-allelic origin of congenital disorder of glycosylation (CDG)-Ic. Hum Genet 106(5):538-45
Westphal V, et al.  (2000) Analysis of multiple mutations in the hALG6 gene in a patient with congenital disorder of glycosylation Ic. Mol Genet Metab 70(3):219-23
Westphal V, et al.  (2000) Reduced heparan sulfate accumulation in enterocytes contributes to protein-losing enteropathy in a congenital disorder of glycosylation. Am J Pathol 157(6):1917-25
Imbach T, et al.  (1999) A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic. Proc Natl Acad Sci U S A 96(12):6982-7