A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major α-Globin Regulatory Element (MCS-R2) and α0-Thalassemia

Publisher： Karger

E-ISSN： 1421-9662|138|1|61-64

ISSN： 0001-5792

Source： Acta Haematologica, Vol.138, Iss.1, 2017-07, pp. : 61-64

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