Mild Beta-Thalassemia intermedia Caused by Compound Heterozygosity for Gγ(Aγδβ)o/β-Thalassemia and Molecular Characterization of the Defect in Four Chinese Families

Publisher: Karger

E-ISSN: 1421-9662|109|4|169-175

ISSN: 0001-5792

Source: Acta Haematologica, Vol.109, Iss.4, 2003-07, pp. : 169-175

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Abstract