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About 4 results

ALLMedicine™ Alg1-cdg (cdg-ik) Center

Research & Reviews  2 results

ALG1-CDG (CDG-Ik)
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...

ALG1-CDG: a new case with early fatal outcome.
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...

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Clinicaltrials.gov  2 results

ALG1-CDG (CDG-Ik)
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...

ALG1-CDG: a new case with early fatal outcome.
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...

see more →