Haemoglobin F, A2, and S levels in subjects with or without sickle cell trait in south-eastern Gabon-Reference-Cited by-同舟云学术

Haemoglobin F, A2, and S levels in subjects with or without sickle cell trait in south-eastern Gabon

Published:2017-02-23 Issue: Volume: Page:1-6
ISSN:1024-5332
Container-title:Hematology
language:en
Short-container-title:Hematology

Author:

Mombo Landry-Erik¹,Mabioko-Mbembo Gaël¹²,Kassa-Kassa Roland-Fabrice²,Ontsitsagui Emmanuel²,Mboui-Ondo Statiana²,Nzé-Kamsi Leatitia¹³,Nkoghé Dieudonné²,Elion Jacques⁴

Affiliation:

1. Laboratoire de Biologie Moléculaire et Cellulaire (LABMC), Université des Sciences et Techniques de Masuku (USTM), Franceville, Gabon

2. Centre International de Recherches Médicales de Franceville (CIRMF), Unité de Recherches et d’Analyses Médicales (URAM), Franceville, Gabon

3. Centre Hospitalier Régional Amissa Bongo (CHRAB), Franceville, Gabon

4. UMR Inserm U1134-Université Paris Diderot/USCP, Institut National de la Transfusion Sanguine, Paris, France

Funder

Centre International de Recherches Médicales

Laboratoire de Biologie Moléculaire et Cellulaire

Publisher

Informa UK Limited

Subject

Hematology,Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/10245332.2017.1292622

Reference25 articles.

1. The Natural History of Sickle Cell Disease

2. Sickle Cell Disease in Africa

3. Association of Variants at BCL11A and HBS1L-MYB with Hemoglobin F and Hospitalization Rates among Sickle Cell Patients in Cameroon

4. Concurrent Sickle-Cell Anemia and α-Thalassemia

5. The Co-Inheritance of Alpha-Thalassemia and Sickle Cell Anemia Is Associated with Better Hematological Indices and Lower Consultations Rate in Cameroonian Patients and Could Improve Their Survival

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