δ0-Thalassemia in cis of βKnossos globin gene: first homozygous description in thalassemia intermedia Libyans and first combination with codon 39 (C→T) in thalassemia intermedia Tunisian patients-Reference-Cited by-同舟云学术

δ0-Thalassemia in cis of βKnossos globin gene: first homozygous description in thalassemia intermedia Libyans and first combination with codon 39 (C→T) in thalassemia intermedia Tunisian patients

Published:2012-01-01 Issue:10 Volume:50 Page:
ISSN:1437-4331
Container-title:Clinical Chemistry and Laboratory Medicine
language:
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Author:

Sahli Chaima Abdelhafidh,Bibi Amina,Ouali Faida,Siala Hajer,Fredj Sondess Hadj,Othmani Rym,Ouenniche Fekria,Cheour Mondher,Fitouri Zohra,Becher Saida Ben,Messaoud Taieb

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Link

https://www.degruyter.com/document/doi/10.1515/cclm-2012-0102/pdf

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1. Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations;Molecular Biology Reports;2021-08

2. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (−CT) (HBB: c.17_18delCT) and δ-globin CD 59 (−a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia;BMC Pediatrics;2019-02-18

3. Fortuitous description of haemoglobin A2’ [δ16 (A13) Gly→Arg (GGC→CGC)] in a Tunisian family: study of the molecular defect and its origin;Annales de biologie clinique;2015-05

4. β-Globin Genes: Mutation Hot-Spots in the Global Thalassemia Belt;Hemoglobin;2014-12-19

5. Hb Knossos: HBB:c.82G>T Associated with HBB:c.315+1G>A Beta Zero Mutation Causes Thalassemia Intermedia;Indian Journal of Hematology and Blood Transfusion;2014-01-31