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Abstract(s)
Background. Thalassemia is a genetic disease that makes part of an
heterogeneous group of mendelian disturbs characterised by a diminution or absence in the production of one of the α or β Haemoglobin A
chains (α2 β2). β-thalassemia is a variance of the thalassemic disease.
This disease is found in many different ethnic groups and is more incident in some geographic areas, like Mediterranic zones where Algarve
is insert.
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Ferrata Storti Foundation