|
Volumn 16, Issue 11, 1999, Pages 669-671
|
Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: An updated nomenclature for CDG
a a a a a a a a a a a a a a a a a a a a more.. |
Author keywords
ALG3; ALG6; DPM1; Metabolic disorder; MGAT2; MPI; PMM2
|
Indexed keywords
ASPARAGINE;
DOLICHOL PHOSPHATE;
GLYCAN;
OLIGOSACCHARIDE;
POLYPEPTIDE;
PROTEIN;
CARBOHYDRATE SYNTHESIS;
CARBOHYDRATE TRANSPORT;
CHEMICAL BOND;
CONGENITAL DISORDER OF GLYCOSYLATION;
ENZYME DEFICIENCY;
GLYCOSYLATION;
HUMAN;
LETTER;
NOMENCLATURE;
PRIORITY JOURNAL;
PROTEIN BINDING;
PROTEIN GLYCOSYLATION;
|
EID: 0033333620
PISSN: 02820080
EISSN: None
Source Type: Journal
DOI: 10.1023/a:1017249723165 Document Type: Letter |
Times cited : (104)
|
References (0)
|