Human Glycosylation Disorders and Sugar Supplement Therapy
- 16 February 1999
- journal article
- review article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 255 (2), 189-193
- https://doi.org/10.1006/bbrc.1998.9945
Abstract
No abstract availableKeywords
This publication has 48 references indexed in Scilit:
- Hereditary fructose intolerance.Journal of Medical Genetics, 1998
- A Novel Disorder of N-Glycosylation Due to Phosphomannose Isomerase DeficiencyBiochemical and Biophysical Research Communications, 1998
- Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.Journal of Clinical Investigation, 1998
- Diseases of abnormal protein glycosylation: an emerging area.Journal of Clinical Investigation, 1998
- Feline Mucopolysaccharidosis Type VI: Correction of Glycosaminoglycan Storage in Myoblasts by Retrovirus-Mediated Transfer of the Feline N-Acetylgalactosamine 4-Sulfatase GeneDNA and Cell Biology, 1997
- Selectin ligands: will the real ones please stand up?Journal of Clinical Investigation, 1997
- Phosphomannomutase deficiency is a cause of carbohydrate‐deficient glycoprotein syndrome type IFEBS Letters, 1995
- Abnormal synthesis of dolichol-linked oligosaccharides in carbohydrate-deficient glycoprotein syndromeGlycobiology, 1995
- Carbohydrate-deficient glycoprotein syndrome: not an N-linked oligosaccharide processing defect, but an abnormality in lipid-linked oligosaccharide biosynthesis?Journal of Clinical Investigation, 1994
- On the biosynthesis of L-fucose and L-fucose metabolism in manBiochimica et Biophysica Acta, 1960