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Autor:
Bárbara C.M.F. Paes, Luiza C.J.R. Stabeli, Péricles N.M. Costa, Maristela Delgado Orellana, Simone Kashima, Dimas Tadeu Covas, Virgínia Picanço-Castro
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss 2, Pp 156-164 (2021)
Introduction: Sickle cell disease (SCD) is a monogenic disease and it is estimated that 300,000 infants are born annually with it. Most treatments available are only palliative, whereas the allogeneic hematopoietic stem cell transplantation offers th
Externí odkaz:
https://doaj.org/article/6cc75d9a477c437197bd6e40b51e1ab7