Carbohydrate-deficient glycoprotein syndrome type V: Deficiency of dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl glucosyltransferase

Proceedings of the National Academy of Sciences of the United States of America

Volumn 95, Issue 22, 1998, Pages 13200-13205

  Körner, Christian ^a   Knauer, Roland ^b   Holzbach, Ulrike ^a   Hanefeld, Folker ^a   Lehle, Ludwig ^b   Von Figura, Kurt ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b UNIVERSITY OF REGENSBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DOLICHOL PHOSPHATE MANNOSE; GLUCOSYLTRANSFERASE; GLYCOPROTEIN; MANNOSE PHOSPHATE ISOMERASE; OLIGOSACCHARIDE; TRANSFERRIN;

ARTICLE; CASE REPORT; CLINICAL FEATURE; CONGENITAL DISORDER OF GLYCOSYLATION; CONTROLLED STUDY; DISEASE CLASSIFICATION; ENZYME ACTIVITY; ENZYME DEFICIENCY; FEMALE; FIBROBLAST; GLYCOSYLATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN CELL; ISOELECTRIC FOCUSING; PRIORITY JOURNAL;

CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME; CELLS, CULTURED; FIBROBLASTS; GLUCOSYLTRANSFERASES; HUMANS; MANNOSE; MANNOSE-6-PHOSPHATE ISOMERASE; METHIONINE; OLIGOSACCHARIDES; PHOSPHOTRANSFERASES (PHOSPHOMUTASES); SKIN;

EID: 0032573176     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.22.13200     Document Type: Article

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