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Autor:
Alexandra Hertz, Lynn Tran, Kari Hale, Angela Coxon, Sandra Ross, Tom Dineen, Stephanie Matyas, Cynthia Hartley, Sean Yoder, Kurt Morgenstern, Park Cindy, Tara Arvedson, John W. Eschelbach, Graham Molineux, Dwight Winters
Publikováno v:
Blood. 120:3263-3263
Abstract 3263 Introduction Sickle cell disease and beta thalassemia are disorders caused by mutations in adult hemoglobin (HbA) or defects in HbA expression. A potential therapeutic solution is reactivation of fetal hemoglobin (HbF) expression. Altho