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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...

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Detalles Bibliográficos
Autor principal: Serjeant, Graham R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602861/
https://www.ncbi.nlm.nih.gov/pubmed/34805213
http://dx.doi.org/10.3389/fmed.2021.745189

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