Mis-sense mutation of α1-antichymotrypsin gene associated with chronic lung disease
- 1 June 1992
- journal article
- letter
- Published by Elsevier in The Lancet
- Vol. 339 (8808) , 1538
- https://doi.org/10.1016/0140-6736(92)91301-n
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Alpha 1-antitrypsin deficiency, emphysema, and liver disease. Genetic basis and strategies for therapy.Journal of Clinical Investigation, 1990
- Pulmonary Function in Middle-aged Women with Heterozygous Deficiency of the Serine Protease Inhibitor Alpha1-AntichymotrypsinAmerican Review of Respiratory Disease, 1990
- Risk of Cirrhosis and Primary Liver Cancer in Alpha1-Antitrypsin DeficiencyNew England Journal of Medicine, 1986
- Familial α1‐Antichymotrypsin DeficiencyActa Medica Scandinavica, 1986