Charles J Waechter Selected Research

Congenital disorder of glycosylation type 1J

8/2003

Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) causes a novel congenital disorder of Glycosylation Type Ij.

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Charles J Waechter Research Topics

Disease

3	Congenital Disorders of Glycosylation 01/2016 - 08/2003
1	Glycogen Storage Disease (Glycogenosis) 01/2021
1	Microcephaly 11/2013
1	Muscle Hypotonia (Hypotonia) 11/2013
1	Muscular Dystrophies (Muscular Dystrophy) 11/2013
1	Typhoid Fever (Typhoid) 01/2012
1	Congenital disorder of glycosylation type 1J 08/2003

Drug/Important Bio-Agent (IBA)

3	Proteins (Proteins, Gene)FDA Link 01/2016 - 08/2003
2	Uridine Diphosphate (UDP)IBA 01/2021 - 08/2003
1	AcetylglucosamineIBA 01/2021
1	GlycogenIBA 01/2021
1	LipidsIBA 01/2016
1	Dystroglycans (Dystroglycan)IBA 11/2013
1	AntibodiesIBA 11/2013
1	CarbohydratesIBA 11/2013
1	Creatine Kinase (Creatine Phosphokinase)IBA 11/2013
1	Polysaccharides (Glycans)IBA 01/2012
1	TransferasesIBA 08/2003
1	OligosaccharidesIBA 08/2003
1	DolicholsIBA 08/2003
1	Phosphates (Orthophosphate)IBA 08/2003