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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

✍ Scribed by Panagoula Kollia; Angelos Kalamaras; Christos Chassanidis; Maria Samara; Nikolaos K. Vamvakopoulos; Milena Radmilovic; Sonja Pavlovic; Manoussos N. Papadakis; George P. Patrinos


Book ID
116304610
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
137 KB
Volume
41
Category
Article
ISSN
1079-9796

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