In the past decade, the identification of most genes involved in Congenital Disorders of Glycosylation (CDG) (type I) was achieved by a combination of biochemical, cell biological and glycobiological investigations. This has been truly successful for CDG-I, because the candidate genes could be selected on the basis of the homology of the synthetic pathway of the dolichol linked oligosaccharide in human and yeast. On the contrary, only a few CDG-II defects were elucidated, be it that some of the discoveries represent wonderful breakthroughs, like e.g, the identification of the COG defects. In general, many rare genetic defects have been identified by positional cloning. However, only a few types of CDG have effectively been elucidated by lin...
Almost 50 inborn errors of metabolism have been described due to congenital defects in N-linked glyc...
Congenital disorders of glycosylation (CDG) arise from pathogenic mutations in over 100 genes leadin...
International audienceCongenital disorders of glycosylation (CDG) are rare autosomal genetic disease...
Congenital disorders of glycosylation type I (CDG-I) form a growing group of recessive neurometaboli...
Congenital disorders of glycosylation (CDG) are inherited autosomal-recessive diseases that impair N...
Congenital disorders of glycosylation (CDG) are a rapidly growing family of genetic diseases that cu...
Congenital disorders of glycosylation type 1 (CDG-I) comprise a group of 27 genetic defects with het...
Glycosylation is one of the most abundant protein modifications found in nature. It results from a m...
Biochemical and biological properties of glycoconjugates are strongly determined by the specific str...
The survey summarizes in its first part the current status of knowledge on the Congenital Disorders ...
International audienceGlycoside hydrolases (GHs) are found in all domains of life, and at least 87 d...
Congenital disorders of glycosylation (CDG) are rare multisystem metabolic diseases and their number...
Glycosylation is one of the most abundant protein modifications found in nature. It results from a m...
Almost 50 inborn errors of metabolism have been described due to congenital defects in N-linked glyc...
Congenital disorders of glycosylation (CDG) arise from pathogenic mutations in over 100 genes leadin...
International audienceCongenital disorders of glycosylation (CDG) are rare autosomal genetic disease...
Congenital disorders of glycosylation type I (CDG-I) form a growing group of recessive neurometaboli...
Congenital disorders of glycosylation (CDG) are inherited autosomal-recessive diseases that impair N...
Congenital disorders of glycosylation (CDG) are a rapidly growing family of genetic diseases that cu...
Congenital disorders of glycosylation type 1 (CDG-I) comprise a group of 27 genetic defects with het...
Glycosylation is one of the most abundant protein modifications found in nature. It results from a m...
Biochemical and biological properties of glycoconjugates are strongly determined by the specific str...
The survey summarizes in its first part the current status of knowledge on the Congenital Disorders ...
International audienceGlycoside hydrolases (GHs) are found in all domains of life, and at least 87 d...
Congenital disorders of glycosylation (CDG) are rare multisystem metabolic diseases and their number...
Glycosylation is one of the most abundant protein modifications found in nature. It results from a m...
Almost 50 inborn errors of metabolism have been described due to congenital defects in N-linked glyc...
Congenital disorders of glycosylation (CDG) arise from pathogenic mutations in over 100 genes leadin...
International audienceCongenital disorders of glycosylation (CDG) are rare autosomal genetic disease...