Genotype-phenotype correlation of HbH disease in northern Iraq

BACKGROUND: HbH disease results from dysfunction of three, less commonly two, α-globin genes through various combinations of deletion and non-deletion mutations. Characterization of the mutations and the underlying genotypes is fundamental for proper screening and prevention of thalassaemia in any r...

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Detalles Bibliográficos
Autores principales: Shamoon, Rawand P., Yassin, Ahmed K., Polus, Ranan K., Ali, Mohamad D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559146/
https://www.ncbi.nlm.nih.gov/pubmed/33059634
http://dx.doi.org/10.1186/s12881-020-01141-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7559146/
https://www.ncbi.nlm.nih.gov/pubmed/33059634
http://dx.doi.org/10.1186/s12881-020-01141-8

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