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 |