Abstract
ObjectivesBeta-thalassemias are one of the commonest genetic hemoglobin disorder. Regular blood transfusions are the cornerstone interventions in the management of thalassemia patients. However, repeated blood transfusion is associated with iron...
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Archives of disease in childhood. Fetal and neonatal edition
Paper Title
Journal
Date
