Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients-Reference-Cited by-同舟云学术

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Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients

Published:2022-09-15 Issue:10 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Mahmoud Taher¹²³^ORCID,Sahli Chaima¹,Hadj Fredj Sondess¹,Amri Yessine¹,Othmani Rim¹,Mohamed Ghaber S.²,Zein Ekhtelbenina⁴,Messaoud Taieb¹

Affiliation:

1. Biochemistry and Molecular Laboratory LR00SP03 Children's Hospital of Tunis Tunis Tunisia

2. Medical Analysis Laboratory (MauriLab) Nouakchott Mauritania

3. Doctoral School (STVST) of the Faculty of Sciences of Tunis University of Tunis El Manar Tunis Tunisia

4. Pediatric Hemato‐Oncology Department of the National Oncology Center (CNO) Nouakchott Mauritania

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.2048

Reference36 articles.

1. Determination of the spectrum of β thalassemia genes in Spain by use of dot blot analysis of amplified β globin DNA;Amselem S.;American Journal of Human Genetics,1988

2. beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site.

3. A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for α-thalassemia

4. HB Siirt [β27(β9)ALA→GLY]: A New, Electrophoretically Silent, Hemoglobin Variant

5. Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem

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