Genotype-phenotype correlation of HbH disease in northern Iraq
Abstract 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...
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Format: | Book |
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BMC,
2020-10-01T00:00:00Z.
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A1234.567 |
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