Sickle Cell Disease: Thoughts for India From the Jamaican Cohort Study
The sickle cell gene in India represents a separate occurrence of the HbS mutation (the Asian haplotype), which has occurred against a genetic background characterised by high levels of fetal haemoglobin and widely varying frequencies of alpha thalassaemia. These features, which tend to inhibit sick...
Guardado en:
Autor principal: | Graham R. Serjeant |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/6b86d2e6106e4c169c426a2a1d638bb2 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Screening for the Sickle Cell Trait in Odisha, India: An Approach to a Major Public Health Burden
por: Basanta Kumar Bindhani, et al.
Publicado: (2021) -
Analyzing effects of sickle cell disease on morphometric and cranial growth in Indian population
por: Kumari Menka, et al.
Publicado: (2021) -
Sickle Cell Anemia and <i>Babesia</i> Infection
por: Divya Beri, et al.
Publicado: (2021) -
Hemoglobin level and macular thinning in sickle cell disease
por: Hussnain SA, et al.
Publicado: (2019) -
In Vitro Red Blood Cell Segregation in Sickle Cell Anemia
por: Viviana Clavería, et al.
Publicado: (2021)