Development of a Quantitative Multiplex PCR to Detect Three Common Alpha Thalassemia Deletions

Author:

Hajimohammadi Zahra12,Alimohammadi-Bidhendi Sara2,Bagheri Amiri Fahimeh3,Karimipoor Morteza2,Davoudi-Dehaghani Elham2ORCID,Entezam Mona1

Affiliation:

1. Department of Medical Genetics, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran

2. Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran

3. Department of Epidemiology and Biostatistics, Research Centre for Emerging and Reemerging Infectious Diseases, Pasteur Institute of Iran, Tehran, Iran

Funder

Pasteur Institute of Iran

Shiraz University of Medical Sciences

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Reference18 articles.

1. Molecular basis of α-thalassemia in Iran;Valaei A;Iran Biomed J,2018

2. Hemoglobinopathies in Iran: an updated review;Nasiri A;Int J Hematol Stem Cell Res,2020

3. Variable Clinical Phenotypes of α-Thalassemia Syndromes

4. Hematologic features of alpha thalassemia carriers;Akhavan-Niaki H;Int J Mol Cell Med,2012

5. A PCR-based strategy to detect the common severe determinants of α thalassaemia

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