A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major α-Globin Regulatory Element (MCS-R2) and α < sup > 0 < /sup > -Thalassemia

Acta Haematol 2017;138:61-64

Source: Acta Haematologica - July 25, 2017 Category: Hematology Source Type: research