Disorders in protein glycosylation and potential therapy: Tip of an iceberg?
- 1 November 1998
- journal article
- review article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 133 (5) , 593-600
- https://doi.org/10.1016/s0022-3476(98)70096-4
Abstract
No abstract availableKeywords
This publication has 50 references indexed in Scilit:
- 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
- A Partial Deficiency of Dehydrodolichol Reduction Is a Cause of Carbohydrate-deficient Glycoprotein Syndrome Type IJournal of Biological Chemistry, 1997
- Phosphomannomutase deficiency is a cause of carbohydrate‐deficient glycoprotein syndrome type IFEBS Letters, 1995
- Carbohydrate-Deficient Glycoprotein Syndrome - A Fourth SubtypeNeuropediatrics, 1995
- Oligosaccharides in vertebrate developmentSeminars in Developmental Biology, 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
- The carbohydrate-deficient glycoprotein syndromes: pre-Golgi and Golgi disorders?Glycobiology, 1993
- Carbohydrate-Deficient Glycoprotein (CDG) Syndrome - A New Variant, Type IIINeuropediatrics, 1993