Genetic variants in the G gamma-globin promoter modulate fetal hemoglobin expression in the Colombian population

Fetal hemoglobin (HbF) is a determining factor for the development of sickle cell anemia. High HbF levels lower the intensity of symptoms of this disease. HbF levels can vary in patients with sickle cell anemia and individuals without the disease.

Autores:
Fong Reales, Cristian Javier
Mendoza Y.
Barreto G.
Tipo de recurso:
Article of journal
Fecha de publicación:
2020
Institución:
Universidad Cooperativa de Colombia
Repositorio:
Repositorio UCC
Idioma:
OAI Identifier:
oai:repository.ucc.edu.co:20.500.12494/42307
Acceso en línea:
https://doi.org/10.3303/CET1649065
https://hdl.handle.net/20.500.12494/42307
Palabra clave:
hemoglobin F
Article
chromosome
Colombian
G gamma globin gene
gene
gene frequency
genetic variability
human
major clinical study
multicenter study
promoter region
protein expression
sickle cell anemia
single nucleotide polymorphism
Rights
closedAccess
License
http://purl.org/coar/access_right/c_14cb