Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC)

Author:

Sahli Chaima Abdelhafidh1,Ben Salem Ikbel1,Jouini Latifa1,Laouini Naouel1,Dabboubi Rym1,Hadj Fredj Sondes1,Siala Hajer1,Othmeni Rym1,Dakhlaoui Boutheina1,Fattoum Slaheddine1,Bibi Amina1,Messaoud Taieb1

Affiliation:

1. Laboratory of Clinical Biochemistry and Molecular Biology; Research Laboratory LR00SP03; Children's Hospital; Tunis Tunisia

Funder

Ministry of Scientific Research and Technology and Competence Development

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Reference25 articles.

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2. Evolution of hemoglobinopathy in Africa: Results, problems and prospect;Fattoum;Medit J Hemat Infect Dis,2009

3. Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS);Newton;Nucleic Acids Res,1989

4. A simple approach to prenatal diagnosis of β-thalassemia in a geographic area where multiple mutations occur;Cai;Blood,1988

5. Reverse dot blot probes for the screening of β-thalassemia mutations in Asians and American blacks;Cai;Hum Mutat,1994

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Molecular heterogeneity of β‐thalassemia variants in the Eastern region of Morocco;Molecular Genetics & Genomic Medicine;2022-05-26

2. Genetics and genomic medicine in Tunisia;Molecular Genetics & Genomic Medicine;2018-03

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