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Published in 2017 at "Hemoglobin"
DOI: 10.1080/03630269.2017.1397016
Abstract: Abstract Previous molecular analyses of α-thalassemia (α-thal) in the Republic of Macedonia have identified the following genetic defects: –α3.7 (rightward), –(α)20.5 and – –MED I deletions and Hb Icaria [α142, Term→Lys (α2), HBA2: c.427T>A] and polyadenylation signal…
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Keywords:
agrinio described;
described patients;
republic macedonia;
cases agrinio ... See more keywords