A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic

Ítems similars

• Degradation of Misfolded Endoplasmic Reticulum Glycoproteins in Saccharomyces cerevisiae Is Determined by a Specific Oligosaccharide Structure
  per: Jakob, Claude A., et al.
  Publicat: (1998)
• Stepwise assembly of the lipid-linked oligosaccharide in the endoplasmic reticulum of Saccharomyces cerevisiae: identification of the ALG9 gene encoding a putative mannosyl transferase.
  per: Burda, P, et al.
  Publicat: (1996)
• A novel carbohydrate-deficient glycoprotein syndrome characterized by a deficiency in glucosylation of the dolichol-linked oligosaccharide.
  per: Burda, P, et al.
  Publicat: (1998)
• Identification and Functional Analysis of a Defect in the Human ALG9 Gene: Definition of Congenital Disorder of Glycosylation Type IL
  per: Frank, Christian G., et al.
  Publicat: (2004)
• Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie
  per: Imbach, Timo, et al.
  Publicat: (2000)