Hb H Disease Caused by a Homozygosity for the AATAAA→ AATAAG Mutation in the Polyadenylation Site of the α2-Globin Gene: Hematological Observations

Abstract
We have identified 7 patients with Hb H disease as homozygotes for a mutation in the polyadenylation site (AATAAA → AATAAG) and have compared their hematological data with those of Hb H

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