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Congenital disorder of glycosylation type 1J

mutationin DPAGT1

Also Known As:

Congenital Disorder of Glycosylation, Type IJ

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Carbohydrate Metabolism
      - Congenital Disorders of Glycosylation: 570
        Congenital disorder of glycosylation type 1J: 1
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Carbohydrate Metabolism
      - Congenital Disorders of Glycosylation: 570
        Congenital disorder of glycosylation type 1J: 1

Experts

1.	Freeze, Hudson H: 1 article (08/2003)
2.	Gilmore, Reid: 1 article (08/2003)
3.	Karaoglu, Denise: 1 article (08/2003)
4.	Krasnewich, Donna: 1 article (08/2003)
5.	Lubinsky, Mark S: 1 article (08/2003)
6.	Rush, Jeffrey S: 1 article (08/2003)
7.	Waechter, Charles J: 1 article (08/2003)
8.	Wu, Xiaohua: 1 article (08/2003)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Congenital disorder of glycosylation type 1J:

1.	Uridine Diphosphate (UDP)IBA 08/01/2003 - "Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) causes a novel congenital disorder of Glycosylation Type Ij."
2.	TransferasesIBA 08/01/2003 - "Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) causes a novel congenital disorder of Glycosylation Type Ij."
3.	Phosphates (Orthophosphate)IBA 08/01/2003 - "Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) causes a novel congenital disorder of Glycosylation Type Ij."
4.	DolicholsIBA 08/01/2003 - "Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) causes a novel congenital disorder of Glycosylation Type Ij."