Add to ORKGCongenital disorders of glycosylation (CDG) have grown enormously since the discovery of the first protein glycosylation defect in 1980, presenting with a broad clinical spectrum. Expansion in number and complexity of the CDG group has even necessitated a new nomenclature. By 2011, the CDG group includes lipid glycosylation disorders and other related processes and almost 50 distinct disorders.status: publishe
Congenital disorders of glycosylation (CDG) are genetic diseases caused by abnormal protein and lipi...
Glycosylation is one of the most abundant protein modifications found in nature. It results from a m...
Congenital disorder of glycosylation type I (CDG I) represent a rapidly growing group of inherited m...
Glycosylation is the most important posttranslational change for proteins. There are more than 100 d...
Almost 50 inborn errors of metabolism have been described due to congenital defects in N-linked glyc...
Item does not contain fulltextPURPOSE OF REVIEW: Congenital disorders of glycosylation (CDG) have gr...
The congenital disorders of glycosylation (CDG) are a rapidly expanding group of metabolic syndromes...
Objective: Congenital defects of glycosylation (CDG) belongs to a group of genetic diseases that lea...
Congenital disorders of glycosylation (CDG) are a group of clinically heterogeneous disorders charac...
Biochemical and biological properties of glycoconjugates are strongly determined by the specifi c st...
Congenital disorders of glycosylation (CDG) are a group of more than 130 inborn errors of metabolism...
The survey summarizes in its first part the current status of knowledge on the Congenital Disorders ...
Congenital disorders of glycosylation (CDG) are rare disor-ders of carbohydrate metabolism in which ...
Glycosylation is a ubiquitous modification of lipids and proteins. Despite the essential contributio...
Congenital disorders of glycosylation (CDG) are a group of genetic disorders that affect protein and...
Congenital disorders of glycosylation (CDG) are genetic diseases caused by abnormal protein and lipi...
Glycosylation is one of the most abundant protein modifications found in nature. It results from a m...
Congenital disorder of glycosylation type I (CDG I) represent a rapidly growing group of inherited m...
Glycosylation is the most important posttranslational change for proteins. There are more than 100 d...
Almost 50 inborn errors of metabolism have been described due to congenital defects in N-linked glyc...
Item does not contain fulltextPURPOSE OF REVIEW: Congenital disorders of glycosylation (CDG) have gr...
The congenital disorders of glycosylation (CDG) are a rapidly expanding group of metabolic syndromes...
Objective: Congenital defects of glycosylation (CDG) belongs to a group of genetic diseases that lea...
Congenital disorders of glycosylation (CDG) are a group of clinically heterogeneous disorders charac...
Biochemical and biological properties of glycoconjugates are strongly determined by the specifi c st...
Congenital disorders of glycosylation (CDG) are a group of more than 130 inborn errors of metabolism...
The survey summarizes in its first part the current status of knowledge on the Congenital Disorders ...
Congenital disorders of glycosylation (CDG) are rare disor-ders of carbohydrate metabolism in which ...
Glycosylation is a ubiquitous modification of lipids and proteins. Despite the essential contributio...
Congenital disorders of glycosylation (CDG) are a group of genetic disorders that affect protein and...
Congenital disorders of glycosylation (CDG) are genetic diseases caused by abnormal protein and lipi...
Glycosylation is one of the most abundant protein modifications found in nature. It results from a m...
Congenital disorder of glycosylation type I (CDG I) represent a rapidly growing group of inherited m...