ALG12-CDG: novel glycophenotype insights endorse the molecular defect
Sign Up to like & getrecommendations! Published in 2019 at "Glycoconjugate Journal"
DOI: 10.1007/s10719-019-09890-2
Abstract: Congenital disorders of glycosylation (CDG) are genetic diseases characterized by deficient synthesis (CDG type I) and/or abnormal processing (CDG type II) of glycan moieties linked to protein and lipids. The impact of the molecular defects… read more here.
Keywords: alg12 cdg; cdg; endorse molecular; serum ... See more keywords