ALLMedicine™ Alg1-cdg (cdg-ik) Center
Research & Reviews 2 results
https://rarediseases.info.nih.gov/diseases/9838/alg1-cdg-cdg-ik
Jun 30th, 2016 - The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs. Orpha Number: 79327 Definition A severe form of congenital disorders of N-linked glycosylation characterized by severe developme...
https://doi.org/10.1016/j.gene.2013.10.013
Gene Rohlfing AK, Rust S et. al.
Oct 25th, 2013 - Congenital disorders of glycosylation (CDG) are a growing group of inherited metabolic disorders where enzymatic defects in the formation or processing of glycolipids and/or glycoproteins lead to variety of different diseases. The deficiency of GD...
Clinicaltrials.gov 2 results
https://rarediseases.info.nih.gov/diseases/9838/alg1-cdg-cdg-ik
Jun 30th, 2016 - The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs. Orpha Number: 79327 Definition A severe form of congenital disorders of N-linked glycosylation characterized by severe developme...
https://doi.org/10.1016/j.gene.2013.10.013
Gene Rohlfing AK, Rust S et. al.
Oct 25th, 2013 - Congenital disorders of glycosylation (CDG) are a growing group of inherited metabolic disorders where enzymatic defects in the formation or processing of glycolipids and/or glycoproteins lead to variety of different diseases. The deficiency of GD...
