Association between sickle cell anemia and alpha thalassemia reveals a high prevalence of the α3.7triplication in congolese patients than in worldwide series-Reference-Cited by-同舟云学术

Association between sickle cell anemia and alpha thalassemia reveals a high prevalence of the α3.7triplication in congolese patients than in worldwide series

Published:2017-03-09 Issue:1 Volume:32 Page:e22186
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J Clin Lab Anal

Author:

Mikobi Tite Minga¹²³,Lukusa Prosper Tshilobo¹⁴⁵⁶,Aloni Michel Ntetani⁷^ORCID,Lumaka Aimé¹⁴⁵⁶,Akilimali Pierre Zalagile⁸,Devriendt Koenraad⁴,Matthijs Gert⁴,Mbuyi Muamba Jean-Marie⁹,Race Valerie⁴

Affiliation:

1. Center for Human Genetics; Faculty of Medicine; University of Kinshasa; Kinshasa Democratic Republic of Congo

2. Department des Sciences de Bases; Laboratory of Biochemistry and Molecular Biology; Faculty of Medicine; University of Kinshasa; Kinshasa Democratic Republic of Congo

3. Sickle Cell Center of Yolo; Kinshasa Democratic Republic of Congo

4. Center for Human Genetics; Katholieke Universiteit te Leuven; Leuven Belgium

5. Department of Pediatrics; University Hospital of Kinshasa; Faculty of Medicine; University of Kinshasa; Kinshasa Democratic Republic of Congo

6. Institut National de Recherche Biomédicale; Kinshasa Democratic Republic of Congo

7. Division of Hemato-oncology and Nephrology; Department of Pediatrics; Faculty of Medicine; University of Kinshasa; Kinshasa Democratic Republic of Congo

8. Division of Biostatistics and Epidemiology; School of Public Health; University of Kinshasa; Kinshasa Democratic Republic of Congo

9. Division of Hemato-Immuno-Rheumatology; Department of Internal Medicine; Faculty of Medicine; University of Kinshasa; Kinshasa Democratic Republic of Congo

Funder

KU Leuven

Publisher

Wiley

Subject

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

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5. Fetal hemoglobin in sickle cell anemia;Akinsheye;Blood,2011

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4. Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries;Journal of Personalized Medicine;2022-03-31

5. Effect of deletions in the α-globin gene on the phenotype severity of β-thalassemia;Hemoglobin;2022-03-04