Molecular basis of the liver and lung disease associated with the α1-antitrypsin deficiency allele M(malton)

Journal of Biological Chemistry

Volumn 264, Issue 23, 1989, Pages 13938-13945

  Curiel, D T ^a   Holmes, M D ^a   Okayama, H ^a   Brantly, M L ^a   Vogelmeier, C ^a   Travis, W D ^a   Stier, L E ^a   Perks, W H ^a   Crystal, R G ^a  

^a NATIONAL HEART LUNG AND BLOOD INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA 1 ANTITRYPSIN DEFICIENCY; CASE REPORT; HEREDITY; HUMAN; LIVER DISEASE; LUNG DISEASE; PRIORITY JOURNAL;

ALLELES; ALPHA 1-ANTITRYPSIN; ALPHA 1-ANTITRYPSIN DEFICIENCY; AMINO ACID SEQUENCE; BASE SEQUENCE; CASE REPORT; CLONING, MOLECULAR; EMPHYSEMA; FEMALE; GENES, STRUCTURAL; HUMAN; LUNG DISEASES; MALE; MIDDLE AGE; MOLECULAR SEQUENCE DATA; NEUTROPHILS; PANCREATIC ELASTASE; PEDIGREE; PLASMIDS; RISK FACTORS; RNA, MESSENGER; SMOKING; SUPPORT, NON-U.S. GOV'T; TRANSCRIPTION, GENETIC;

EID: 0024348446     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)