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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...
Uloženo v:
| Vydáno v: | BMC Med Genet |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7559146/ https://ncbi.nlm.nih.gov/pubmed/33059634 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01141-8 |
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