Human artificial chromosome-mediated genetic correction of human dystrophic skeletal muscle progenitors for the autologous cell therapy of Duchenne muscular dystrophy
Human artificial chromosome-mediated genetic correction of human dystrophic skeletal muscle progenitors for the autologous cell therapy of Duchenne muscular dystrophy
复制标题
人类人工染色体介导的人类营养不良骨骼肌祖细胞的遗传校正,用于杜氏肌营养不良症的自体细胞治疗
作者:
Benedetti S.