Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene Cluster-Reference-Cited by-同舟云学术

Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene Cluster

Published:2022-05-04 Issue:3 Volume:46 Page:168-175
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Manco Licínio¹^ORCID,Santos Raquel²³⁴,Rocha Catarina²³⁴,Relvas Luís⁵,Bento Celeste¹⁵^ORCID,Maia Tabita⁵,Gomes Verónica²³^ORCID,Amorim António²³⁴^ORCID,Prata Maria J.²³⁴^ORCID

Affiliation:

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

2. Institute of Investigation and Innovation in Health (i3S), University of Porto, Porto, Portugal

3. Institute of Molecular Pathology and Immunology (IPATIMUP), University of Porto, Porto, Portugal

4. Department of Biology, Faculty of Sciences, University of Porto, Porto, Portugal

5. Department of Haematology, Coimbra Hospital and University Centre (CHUC), Coimbra, Portugal

Funder

FEDER

FCT

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2022.2070498

Reference26 articles.

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

2. Molecular basis of β thalassemia and potential therapeutic targets

3. Manipulation of Developmental Gamma-Globin Gene Expression: an Approach for Healing Hemoglobinopathies

4. Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults

5. Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of -thalassemia

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