β-Trace protein in human cerebrospinal fluid: A diagnostic marker for N-glycosylation defects in brain

Biochimica et Biophysica Acta - Molecular Basis of Disease

Volumn 1455, Issue 1, 1999, Pages 54-60

  Grünewald, Stephanie ^a,c   Huyben, Karin ^a   De Jong, Jan G N ^a   Smeitink, Jan A M ^a   Rubio, Estella ^a   Boers, Godfried H J ^a   Conradt, Harald S ^b   Wendel, Udo ^c   Wevers, Ron A ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b HELMHOLTZ CENTRE FOR INFECTION RESEARCH   (Germany)

^c HEINRICH HEINE UNIVERSITY   (Germany)

Author keywords

Brain type glycosylation; Carbohydrate deficient glycoprotein syndrome; CDGS type I; Human trace protein; Phosphomannomutase deficiency

Indexed keywords

BETA TRACE PROTEIN; GLYCOPROTEIN; TRANSFERRIN; UNCLASSIFIED DRUG;

ARTICLE; CENTRAL NERVOUS SYSTEM; CEREBROSPINAL FLUID; CHILD; CLINICAL ARTICLE; CONGENITAL DISORDER OF GLYCOSYLATION; CONTROLLED STUDY; DIAGNOSTIC VALUE; HUMAN; INFANT; ISOELECTRIC FOCUSING; PRIORITY JOURNAL; PROTEIN GLYCOSYLATION; SCREENING; TRANSFERRIN BLOOD LEVEL;

ADOLESCENT; ADULT; BIOLOGICAL MARKERS; BRAIN DISEASES; CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME; CHILD; CHILD, PRESCHOOL; GLYCOSYLATION; HUMANS; INFANT; INTRAMOLECULAR OXIDOREDUCTASES; PROTEIN ISOFORMS;

EID: 0344604283     PISSN: 09254439     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4439(99)00078-2     Document Type: Article

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