A rare AAT variant presenting in a COPD patient: Q0 amersfoort mutation-Reference-Cited by-同舟云学术

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A rare AAT variant presenting in a COPD patient: Q0 amersfoort mutation

Published:2024 Issue: Volume:51 Page:102084
ISSN:2213-0071
Container-title:Respiratory Medicine Case Reports
language:en
Short-container-title:Respiratory Medicine Case Reports

Author:

Tural Önür Seda^ORCID,Karaca Şenkal Kardelen

Publisher

Elsevier BV

Reference16 articles.

1. Clinical practice. Alpha1-antitrypsin deficiency;Silverman;N. Engl. J. Med.,2009

2. American Thoracic Society/European Respiratory Society statement: standards for the diagnosis and management of individuals with alpha-1 antitrypsin deficiency;Am. J. Respir. Crit. Care Med.,2003

3. Alpha1-Antitrypsin deficiency;Strnad;N. Engl. J. Med.,2020

4. α1-Antitrypsin deficiency;Hatipoğlu;Clin. Chest Med.,2016

5. Standards in Diagnostik und Therapie bei Patienten mit Alpha-1-Antitrypsin-Mangel [American Thoracic Society/European Respiratory Society Statement: Standards for the diagnosis and management of individuals with alpha-1 antitrypsin deficiency];Stoller;Pneumologie,2005

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