Genetic diversity from a limited repertoire of mutations on different common allelic backgrounds: α1-antitrypsin deficiency variant Pduarte
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference31 articles.
1. Diagnosis and Treatment of α1-Antitrypsin Deficiency
2. Use of a Highly Purified α1-Antitrypsin Standard to Establish Ranges for the Common Normal and Deficient α1-Antitrypsin Phenotypes
3. Pi M4: An additional Pi M subtype
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2. Novel SERPINA1 Alleles Identified Through a Large Alpha-1 Antitrypsin Deficiency Screening Program and Review of Known Variants;Chronic Obstructive Pulmonary Diseases: Journal of the COPD Foundation;2023
3. Known Mutations at the Cause of Alpha-1 Antitrypsin Deficiency an Updated Overview of SERPINA1 Variation Spectrum;The Application of Clinical Genetics;2021-03
4. Las alteraciones en el pico de fusión de las sondas de hibridación usadas para el genotipado en la deficiencia de alfa-1 antitripsina no siempre implican errores;Archivos de Bronconeumología;2019-06
5. Changes in the Melting Peak of Hybridization Probes Used for Genotyping in Alpha-1 Antitrypsin Deficiency Do Not Always Imply Errors;Archivos de Bronconeumología (English Edition);2019-06
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