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Autor:
John P. Galvin, Santosh L. Saraf, Damiano Rondelli, Victor R. Gordeuk, Shivi Jain, Robert E. Molokie, Karen Sweiss, Michel Gowhari, John G. Quigley, Irum Khan, Pritesh R. Patel, David Peace, Krishna Ghimire
Publikováno v:
Blood. 132:313-313
Sickle cell disease (SCD) is an inherited red blood cell disorder that leads to substantial morbidity and a heavy burden on the health care system. Nonmyeloablative allogeneic hematopoietic stem cell transplantation (HSCT) regimens using HLA-matched