Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Samir Silavizadeh"'
Autor:
Roza Kamfiroozi, Samir Silavizadeh, Marzieh Bardestani, Mohammadreza Bordbar, Sezaneh Haghpanah, Mehran Karimi
Publikováno v:
Iranian Red Crescent Medical Journal
Background: β-Thalassemia is an inherited hemoglobin disorder caused by defective synthesis of s-globin chains. Hemoglobin (Hb) F induction is a possible therapeutic approach which can partially compensate for α and non-α globin chains imbalance.
Publikováno v:
Haemophilia. 19:e177-e178