Cytochrome b deficiency in an autosomal form of chronic granulomatous disease: a third form of chronic granulomatous disease recognized by monocyte hybridization
- Author
- WEENING, R. S1 ; CORBEEL, L; DE BOER, M; LUTTER, R; VAN ZWIETEN, R; HAMERS, M. N; ROOS, D
[1] Univ. Amsterdam, acad. medical center, Amsterdam, Netherlands - Source
The Journal of clinical investigation. 1985, Vol 75, Num 3, pp 915-920 ; ref : 25 ref
- CODEN
- JCINAO
- ISSN
- 0021-9738
- Scientific domain
- General medicine general surgery
- Publisher
- American Society for Clinical Investigation, Ann Arbor, MI
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Caractère autosomique Chronique Cytochrome c Déficit Granulomatose Hybridation cellulaire Hémopathie Leucocyte maladie Monocyte Pédiatrie
- Keyword (en)
- Autosomal character Chronic Cytochrome c Deficiency Granulomatosis Cell hybridization Hemopathy Leukocyte disease Monocyte Pediatrics
- Keyword (es)
- Cronico Deficit Monocito Pediatria
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19D Other diseases. Hematologic involvement in other diseases
- Discipline
- Blood diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 9122138
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
10.1172/JCI111792 
https://dx.doi.org/10.1172/JCI111792
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