Molecular heterogeneity of C2 deficiency
- Author
- JOHNSON, C. A1 ; DENHSEN, P; WETSEL, R. A; COLE, F. S; GOEKEN, N. E; COLTEN, H. R
[1] Washington univ. school medicine, Edward Mallinckrodt dep. pediatrics, Saint Louis MO, United States - Source
The New England journal of medicine. 1992, Vol 326, Num 13, pp 871-874 ; ref : 19 ref
- CODEN
- NEJMAG
- ISSN
- 0028-4793
- Scientific domain
- General medicine general surgery
- Publisher
- Massachusetts Medical Society, Boston, MA
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Biologie moléculaire Complément C2 Déficit Homme Maladie héréditaire Métabolisme pathologie
- Keyword (en)
- Molecular biology Complement C2 Deficiency Human Genetic disease Metabolic diseases
- Keyword (es)
- Biología molecular Complemento C2 Déficiencia Hombre Enfermedad hereditaria Metabolismo patología
- Classification
- Discipline
- Metabolic diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5275461
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
10.1056/NEJM199203263261306 
https://dx.doi.org/10.1056/NEJM199203263261306
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