Genetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift β-Thalassemia Mutation [HBB: c.265_266del; p.Leu89Glufs*2]-Reference-Cited by-同舟云学术

Genetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift β-Thalassemia Mutation [HBB: c.265_266del; p.Leu89Glufs*2]

Published:2017-03-04 Issue:2 Volume:41 Page:89-95
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Gueye Tall Fatou¹²³,Martin Cyril²⁴,Malick Ndour El Hadji¹³,Déme Ly Indou³⁵,Renoux Céline⁶²,Chillotti Louis⁶,Veyrenche Nicolas⁶,Connes Philippe²⁴⁷,Madieye Gueye Papa¹,Ndiaye Diallo Rokhaya¹,Lacan Philippe⁶,Diagne Ibrahima⁵⁸,Amadou Diop Pape¹,Cissé Aynina¹,Lopez Sall Philomène¹³,Joly Philippe⁶²⁴

Affiliation:

1. Laboratoire de Biochimie Pharmaceutique-FMPO, Université Cheikh Anta Diop, Dakar, Sénégal;

2. Laboratoire Interuniversitaire de Biologie de la Motricité (LIBM) EA7424, Equipe ‘Biologie Vasculaire et du Globule Rouge,’ Université Claude Bernard Lyon 1, COMUE Lyon, France;

3. Centre Hospitalier National d’Enfants Albert-Royer, Dakar, Sénégal;

4. Laboratoire d’Excellence sur le Globule Rouge (Labex GR-Ex), Paris, France;

5. Service Universitaire de Pédiatrie-FMPO, Université Cheikh Anta Diop, Dakar, Sénégal;

6. UF Pathologie Moléculaire du Globule Rouge, Laboratoire de Biochimie et Biologie Moléculaire Grand-Est, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France;

7. Institut Universitaire de France, Paris, France

8. UFR des Sciences de la Santé, Université Gaston Berger, Saint-Louis, Sénégal;

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2017.1339610

Reference43 articles.

1. Global epidemiology of sickle haemoglobin in neonates: a contemporary geostatistical model-based map and population estimates

2. A network model to predict the risk of death in sickle cell disease

3. Alpha-thalassaemia promotes frequent vaso-occlusive crises in children with sickle cell anaemia through haemorheological changes

4. Coinheritance of α-Thalassemia Decreases the Risk of Cerebrovascular Disease in a Cohort of Children with Sickle Cell Anemia

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