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Table 5 Distribution of the Ggamma -158 C→T and AgammaT mutations in thalassemic patients and in control subjects.

From: Factors regulating Hb F synthesis in thalassemic diseases

GROUP OF PATIENTS Allele frequencies
  Ggamma-158 C→T AgammaT
Sub-silent beta tal int 8.6 27.3
Evident beta tal int 18.3 26.6
beta tal int with genotype triplicated alpha + beta tal 16.6 17.6
Hb H disease 37.5 5.5
Tal major 2.1 35.4
Normal controls 25.0 18.0