Long-standing mild hypertransaminasaemia caused by congenital disorder of glycosylation (CDG) type IIx

Journal of Inherited Metabolic Disease

Volumn 31, Issue SUPPL. 2, 2008, Pages

  Calvo, P L ^a   Pagliardini, S ^a   Baldi, M ^a   Pucci, A ^a   Sturiale, L ^b   Garozzo, D ^b   Vinciguerra, T ^a   Barbera, C ^a   Jaeken, J ^c  

^a UNIVERSITY OF TURIN   (Italy)

^b CNR   (Italy)

^c UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; BIOLOGICAL MARKER;

ADULT; BLOOD; CASE REPORT; CONGENITAL DISORDER OF GLYCOSYLATION; ENZYME ASSAY; GENETICS; HUMAN; MALE; PREDICTIVE VALUE; REVIEW; TIME; UPREGULATION;

ADULT; ALANINE TRANSAMINASE; ASPARTATE AMINOTRANSFERASES; BIOLOGICAL MARKERS; CLINICAL ENZYME TESTS; CONGENITAL DISORDERS OF GLYCOSYLATION; HUMANS; MALE; PREDICTIVE VALUE OF TESTS; TIME FACTORS; UP-REGULATION;

EID: 84855609312     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-008-1004-9     Document Type: Article

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