Congenital disorders of N-glycosylation including diseases associated with O- as well as N-glycosylation defects
- Author
- LEROY, Jules G1
[1] Departments of Pediatrics and Medical Genetics, Ghent University School of Medicine and University Hospital, 9000 Ghent, Belgium - Source
Pediatric research. 2006, Vol 60, Num 6, pp 643-656, 14 p ; ref : 98 ref
- CODEN
- PEREBL
- ISSN
- 0031-3998
- Scientific domain
- Genetics; Pediatrics
- Publisher
- Lippincott Williams & Wilkins, Hagerstown, MD
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Association Défaut Glycoprotéine Glycosylation Hypoglycosylation syndrome Pédiatrie Enzymopathie Maladie héréditaire Métabolisme pathologie Système nerveux pathologie
- Keyword (en)
- Association Defect Glycoprotein Glycosylation Carbohydrate deficient glycoprotein syndrome Pediatrics Enzymopathy Genetic disease Metabolic diseases Nervous system diseases
- Keyword (es)
- Asociación Defecto Glicoproteína Glicosilación Carbohydrate deficient glycoprotein syndrome Pediatría Enzimopatía Enfermedad hereditaria Metabolismo patología Sistema nervioso patología
- Classification
- Discipline
- Generalities in medical sciences
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18329183
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1203/01.pdr.0000246802.57692.ea 
https://dx.doi.org/10.1203/01.pdr.0000246802.57692.ea
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