Hb H Disease Caused by a Homozygosity for the AATAAA→ AATAAG Mutation in the Polyadenylation Site of the α2-Globin Gene: Hematological Observations
- 1 January 1992
- journal article
- case report
- Published by S. Karger AG in Acta Haematologica
- Vol. 88 (2-3) , 82-85
- https://doi.org/10.1159/000204657
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 HKeywords
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