An (A)γ type of nondeletional hereditary persistence of fetal hemoglobin with a T → C mutation at position -175 to the cap site of the (A)γ globin gene

T. A. Stoming, G. S. Stoming, K. D. Lanclos, Y. J. Fei, C. Altay, F. Kutlar, T. H.J. Huisman

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