Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15)-Reference-Cited by-同舟云学术

Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15)

Published:2019-09-03 Issue:4-5 Volume:43 Page:223-228
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Abdaoui Wissem¹,Benouareth Djamel Eddine¹,Djenouni Amel²,Renoux Celine³⁴,Grifi Fatiha²,Gouri Adel²,Athamnia Fateh⁵⁶,Benalioua Manel²,Joly Philippe³⁴

Affiliation:

1. Département de Biologie, Faculté des Sciences de la Nature et de la Vie et Sciences de la Terre et de l’Univers, Université 8 mai 1945, BP 401 Guelma 24000, Algérie;

2. Service D’Hématologie, Centre Hospitalo-Universitaire D’Annaba, Annaba, Algérie;

3. Unité Fonctionnelle 34445 ‘Biochimie Des Pathologies Érythrocytaires,’ Laboratoire de Biochimie et Biologie Moléculaire Grand-Est, Hospices Civils de Lyon, Bron, France;

4. Laboratoire Interuniversitaire de Biologie de la Motricité (LIBM) EA7424, Equipe «Biologie vasculaire du globule rouge», Université Claude Bernard Lyon 1, Université de Lyon, Lyon, France;

5. Service d’épidémiologie, Direction de Santé Publique, Guelma, Algérie;

6. Laboratoire de Biochimie, Collège de Médecine, Annaba 23000, Algérie

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2019.1675689

Reference29 articles.

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2. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies

3. ?-Thalassemia in Algeria

4. The spectrum of β-thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy

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