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doi: 10.3389/fimmu.2022.929289 163 DentonCPKhannaD
RandallGWGanttPAPoe-ZeiglerRLBergmannCANoelMEStrawbridgeWRet al
Over the last couple of decades, there has been a spectacular growth of such strategies, setting the scene for developing therapies that could precisely genetically correct a single base mutation in patient with SCD
10.1111/j.1462-5822.2004.00361.x Cell
