INTERMEDIATE ALPHA1-ANTITRYPSIN DEFICIENCY RESULTING FROM A NULL GENE (M-PHENOTYPE).
- Author
- LIEBERMAN J; GAIDULIS L; SCHLEISSNER LA
CITY HOPE MED. CENT., DUORTE, CALIF. 91010 - Source
- CHEST; U.S.A.; DA. 1976; VOL. 70; NO 4; PP. 532-535; BIBL. 16 REF.
- Document type
- Article
- Language
- English
- Keyword (fr)
- DEFICIT HEREDITAIRE EMPHYSEME POUMON ALLELE SILENCIEUX GLYCOPROTEINE ANOMALIE PROTEINE SERIQUE HOMME METABOLISME PATHOLOGIE ALPHA 1 ANTITRYPSINE PNEUMOLOGIE
- Keyword (en)
- DEFICIENCY HEREDITARY EMPHYSEMA LUNG SILENT ALLELE GLYCOPROTEINS ABNORMAL BLOOD PROTEIN HUMAN METABOLIC DISEASES PNEUMOLOGY
- Keyword (es)
- NEUMOLOGIA
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B12 Cardiology. Vascular system
- Discipline
- Cardiology. Circulatory system
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL7750156723
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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