Carbohydrate-deficient glycoprotein syndrome (CDGS) type Ib. A hereditary metabolic disease and its therapy;Carbohydrate-deficient Glycoprotein-Syndrom (CDGS) Typ Ib. Eine hereditäre Stoffwechselerkrankung und ihre Therapie.

MMW Fortschritte der Medizin

Volumn 142, Issue 3 Suppl, 2000, Pages 171-172

  Niehues, R ^a   Hasilik, M ^a  

^a UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

MANNOSE; MANNOSE PHOSPHATE ISOMERASE;

ARTICLE; CONGENITAL DISORDER OF GLYCOSYLATION; GENETICS; HETEROZYGOTE DETECTION; HUMAN;

CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME; HETEROZYGOTE DETECTION; HUMANS; MANNOSE; MANNOSE-6-PHOSPHATE ISOMERASE;

EID: 0034688060     PISSN: 14383276     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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