Combined and differential effects of alpha‐thalassemia and HbF‐quantitative trait loci in Senegalese hydroxyurea‐free children with sickle cell anemia - Concepedia

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Combined and differential effects of alpha‐thalassemia and HbF‐quantitative trait loci in Senegalese hydroxyurea‐free children with sickle cell anemia

12

Citations

35

References

2019

Year

Fatou Guèye Tall, Cyril Martin, El Hadji Malick Ndour, Céline Renoux, Indou Déme Ly, Philippe Connes, Papa Madièye Guéye, Rokhaya Ndiaye Diallo, Ibrahima Diagne, Pape Amadou Diop,

Pediatric Blood & Cancer

Abstract

Alpha-thalassemia -3.7 kb deletion and HbF-QTL are modulating factors of SCA clinical severity that interact with each other. They should be studied and interpreted together and not separately, at least in HU-free children.

References

	Year	Citations

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