Carbohydrate-deficient glycoprotein syndrome type 1; a recently described hereditary metabolic disorder;CDGS-1 - En nyupptäckt ärftlig metabolisk sjukdom: Manifestationer från många organ, incidens 1/80 000, svårbehandlad

Lakartidningen

Volumn 95, Issue 50, 1998, Pages 5742-5748

  Kristiansson, Bengt ^a   Stibler, Helena ^b   Hagberg, Bengt ^a   Wahlström, Jan ^a  

^a SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

^b KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; CONGENITAL DISORDER OF GLYCOSYLATION; GENETICS; HUMAN; INCIDENCE; INFANT; ISOELECTRIC FOCUSING; MORTALITY; NEWBORN; PRENATAL DIAGNOSIS; PRESCHOOL CHILD; REVIEW; SWEDEN; WESTERN BLOTTING;

ADOLESCENT; ADULT; BLOTTING, WESTERN; CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME; CHILD, PRESCHOOL; HUMANS; INCIDENCE; INFANT; INFANT, NEWBORN; ISOELECTRIC FOCUSING; PRENATAL DIAGNOSIS; SWEDEN;

EID: 0032501263     PISSN: 00237205     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (20)

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