DNA polymorphisms at BCL11A, HBS1L-MYB and Xmn1-HBG2 site loci associated with fetal hemoglobin levels in sickle cell anemia patients from Northern Brazil-Reference-Cited by-同舟云学术

DNA polymorphisms at BCL11A, HBS1L-MYB and Xmn1-HBG2 site loci associated with fetal hemoglobin levels in sickle cell anemia patients from Northern Brazil

Published:2014-12 Issue:4 Volume:53 Page:176-179
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Cardoso Greice Lemos,Diniz Isabela Guerreiro,Martins da Silva Aylla Núbia Lima,Cunha Daniele Almeida,da Silva Junior Josivaldo Soares,Carvalho Uchôa Camila Tavares,dos Santos Sidney Emanuel Batista,Trindade Saide Maria Sarmento,Cardoso Maria do Socorro de Oliveira,Guerreiro João Farias

Funder

Universidade Federal do Pará (UFPA)

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference19 articles.

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2. Genetic modifiers of sickle cell disease;Steinberg;Am. J. Hematol.,2012

3. Control of fetal hemoglobin: new insights emerging from genomics and clinical implications;Thein;Hum. Mol. Genet.,2009

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

5. Interethnic admixture and the evolution of Latin American populations;Salzano;Genet Mol Biol,2014

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