✦ LIBER ✦
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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