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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2020
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| 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 |