Mutation detection in the alpha-1 antitrypsin gene (PI) using denaturing gradient gel electrophoresis
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference19 articles.
1. Molecular structure and sequence homology of a gene related to α1-antitrypsin in the human genome
2. A program for selecting DNA fragments to detect mutations by denaturing gel electrophoresis methods
3. Denaturing gradient gel electrophoresis of the α1-antitrypsin gene: Application to prenatal diagnosis
4. PRENATAL DIAGNOSIS OF α1-ANTITRYPSIN DEFICIENCY BY RESTRICTION FRAGMENT LENGTH POLYMORPHISMS, AND COMPARISON WITH OLIGONUCLEOTIDE PROBE ANALYSIS
5. Cloning and characterization of an α1-antitrypsin like gene 12 kb downstream of the genuine α1-antitrypsin gene
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1. Leveraging Population Genomics for Individualized Correction of the Hallmarks of Alpha-1 Antitrypsin Deficiency;Chronic Obstructive Pulmonary Diseases: Journal of the COPD Foundation;2020
2. Rapid detection of Mmalton α1-antitrypsin deficiency allele by real-time PCR and melting curves in whole blood, serum and dried blood spot samples;Clinical Chemistry and Laboratory Medicine (CCLM);2016-01-01
3. The effect of temperature on electrochemically driven denaturation monitored by SERS;Bioelectrochemistry;2015-12
4. Diagnosis of alpha-1 antitrypsin deficiency: Modalities, indications and diagnosis strategy;Revue des Maladies Respiratoires;2014-10
5. WITHDRAWN: Diagnostic du déficit en alpha-1-antitrypsine : les moyens, les indications et la stratégie diagnostique;Revue des Maladies Respiratoires;2014-02
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