Publication | Closed Access

Gγ-196 C→T, Aγ-201 C→T: Two novel mutations in the promoter region of the γ-globin genes associated with nondeletional hereditary persistence of fetal hemoglobin in Greece

Developmental BiologyPromoter RegionGenetic Disorderγ-Globin GenesGeneticsHematologyMolecular GeneticsMedical GeneticsDisease Gene IdentificationMedicineGγ-196 C→tClinical Genetics