A Family Study of the Variability of Pulmonary Function in α1-Antitrypsin Deficiency: Quantitative Phenotypes-Reference-Cited by-同舟云学术

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A Family Study of the Variability of Pulmonary Function in α1-Antitrypsin Deficiency: Quantitative Phenotypes

Published:1990-11 Issue:5 Volume:142 Page:1015-1021
ISSN:0003-0805
Container-title:American Review of Respiratory Disease
language:en
Short-container-title:Am Rev Respir Dis

Author:

Silverman Edwin K.,Province Michael A.,Rao D. C.,Pierce John A.,Campbell Edward J.

Publisher

American Thoracic Society

Subject

Pulmonary and Respiratory Medicine

Reference22 articles.

1. The Alpha1-antitrypsin Gene and Its Mutations

2. Antitrypsin and Emphysema

3. DNA haplotypes. Am J Hum Genet 1989; 44:

4. Report of nomenclature meeting for α1-antitrypsin

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1. Atteinte pulmonaire du déficit en alpha-1 antitrypsine. Recommandations pratiques pour le diagnostic et la prise en charge;Revue des Maladies Respiratoires;2022-09

2. Recent advancements in understanding the genetic involvement of alpha-1 antitrypsin deficiency associated lung disease: a look at future precision medicine approaches;Expert Review of Respiratory Medicine;2022-01-13

3. α1‐Antitrypsin Deficiency;The Liver;2020-01-24

4. Why is Disease Penetration So Variable? Role of Genetic Modifiers of Lung Function in Alpha-1 Antitrypsin Deficiency;Chronic Obstructive Pulmonary Diseases: Journal of the COPD Foundation;2020

5. Hereditary Pulmonary Emphysema;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2020

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