Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and β-thalassemia or Hb Sabine confirms the functional role of the Aγ −158 C>T mutation in γ-globin gene transcription
Titel:
Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and β-thalassemia or Hb Sabine confirms the functional role of the Aγ −158 C>T mutation in γ-globin gene transcription
Auteur:
Kollia, Panagoula Kalamaras, Angelos Chassanidis, Christos Samara, Maria Vamvakopoulos, Nikolaos K. Radmilovic, Milena Pavlovic, Sonja Papadakis, Manoussos N. Patrinos, George P.