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Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and beta-thalassemia or Hb Sabine confirms the functional role of the A gamma-158 C > T mutation in gamma-globin gene transcription

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Συγγραφέας
Kollia, P.; Kalamaras, A.; Chassanidis, C.; Samara, M.; Vamvakopoulos, N. K.; Radmilovic, M.; Pavlovic, S.; Papadakis, M. N.; Patrinos, G. P.
Ημερομηνία
2008
DOI
Λέξη-κλειδί
Εμφάνιση Μεταδεδομένων
URI
http://hdl.handle.net/11615/29534
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