TY  - GEN
AU  - Vabres,P
AU  - Sevin,C
AU  - Amoric,J C
AU  - Odièvre,M H
AU  - Saudubray,J M
AU  - de Prost,Y
TI  - [Skin manifestations of protein glycosylation deficiency, the CDG (carbohydrate deficient glycoprotein) type 1 syndrome]
SN  - 0151-9638
PY  - 1998///1221
KW  - Acyl Carrier Protein
KW  - metabolism
KW  - Biopsy
KW  - Congenital Disorders of Glycosylation
KW  - diagnosis
KW  - Diagnosis, Differential
KW  - Glycosylation
KW  - Humans
KW  - Infant
KW  - Liver
KW  - pathology
KW  - Male
KW  - Phosphoglucomutase
KW  - Phosphotransferases (Phosphomutases)
KW  - deficiency
KW  - Skin Diseases
N1  - Publication Type: Case Reports; English Abstract; Journal Article
ER  -