Variantes genéticas asociadas con niveles de hemoglobina fetal muestran diversos orígenes étnicos en pacientes colombianos con anemia falciforme
etal hemoglobin is an important factor in modulating the severity of sickle cell anemia. Its level in peripheral blood underlies strong genetic determination. Associated loci with increased levels of fetal hemoglobin display population-specific allele
- Autores:
-
Fong Reales, Cristian javier
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2023
- Institución:
- Universidad Cooperativa de Colombia
- Repositorio:
- Repositorio UCC
- Idioma:
- OAI Identifier:
- oai:repository.ucc.edu.co:20.500.12494/50623
- Acceso en línea:
- https://doi.org/10.7705/biomedica.v35i3.2573
https://revistabiomedica.org/index.php/biomedica/article/view/2573
https://hdl.handle.net/20.500.12494/50623
- Palabra clave:
- BCL11A
BETA-GLOBIN CLUSTER
FETAL HEMOGLOBIN
HBS1L-MYB.
POLYMORPHISM
SICKLE CELL; ADMIXTURE
SINGLE NUCLEOTIDE; ANEMIA
- Rights
- openAccess
- License
- http://purl.org/coar/access_right/c_abf2
| Summary: | etal hemoglobin is an important factor in modulating the severity of sickle cell anemia. Its level in peripheral blood underlies strong genetic determination. Associated loci with increased levels of fetal hemoglobin display population-specific allele |
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