Heterozygosity of α1-Antitrypsin: A Health Risk?
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,General Biochemistry, Genetics and Molecular Biology
Link
http://www.tandfonline.com/doi/pdf/10.3109/10408368909114595
Reference191 articles.
1. Genes for immunoglobulin heavy chains and for α1-antitrypsin are localized to specific regions of chromosome 14q
2. Amino acid substitution Glu→Lys in α1-antitrypsin PiZ
3. Identification of a second mutation in the protein-coding sequence of the Z type alpha 1-antitrypsin gene.
4. α 1 -Antitrypsin Deficiency: A Variant with No Detectable α 1 -Antitrypsin
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1. Massive ascites and the heterozygous alpha 1 antitrypsin (α1 AT) living related donor liver in the homozygous child;Pediatric Transplantation;2017-10-15
2. Alpha-1 Antitrypsin PiMZ Genotype Is Associated with Chronic Obstructive Pulmonary Disease in Two Racial Groups;Annals of the American Thoracic Society;2017-08
3. Cryptogenic Chronic Hepatitis and Its Changing Guise in Adults;Digestive Diseases and Sciences;2011-06-07
4. Longitudinal Decline of Diffusing Capacity of the Lung for Carbon Monoxide in Community Subjects With the PiMZ α 1 -Antitrypsin Phenotype;Chest;2008-05
5. Alpha-1-antitrypsin (AAT) anomalies are associated with lung disease due to rapidly growing mycobacteria and AAT inhibits Mycobacterium abscessus infection of macrophages;Scandinavian Journal of Infectious Diseases;2007-01
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