Multi-Locus Models to Address Hb F Variability in Portuguese β-Thalassemia Carriers-Reference-Cited by-同舟云学术

Multi-Locus Models to Address Hb F Variability in Portuguese β-Thalassemia Carriers

Published:2020-03-03 Issue:2 Volume:44 Page:113-117
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Manco Licínio¹²^ORCID,Bento Celeste¹²^ORCID,Relvas Luís²,Cunha Elisabete²,Pereira Janet²,Moreira Valeria¹,Alvarez Manuela¹,Maia Tabita²,Ribeiro M. Letícia¹²^ORCID

Affiliation:

1. Research Centre for Anthropology and Health (CIAS), Department of Life Sciences, University of Coimbra, Coimbra, Portugal;

2. Department of Haematology, Centro Hospitalar e Universitário de Coimbra (CHUC), Coimbra, Portugal

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2020.1753766

Reference27 articles.

1. Discovering the genetics underlying foetal haemoglobin production in adults

2. Genetic Basis and Genetic Modifiers of β-Thalassemia and Sickle Cell Disease

3. Molecular basis of β thalassemia and potential therapeutic targets

4. Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.

5. The modifying effect of Xmn1-HBG2 on thalassemic phenotype is associated with its linked elements in the beta globin locus control region, including the palindromic site at 5′HS4

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