对状细胞疾病的基因疗法的进展:从临床前创新到临床实施和获取挑战

Henna Butt1,2, Mamatha Mandava1,2, David Jacobsohn1,2

  • 1Cancer and Blood Disorders Center, Children's National Hospital, Washington, District of Columbia, USA.

The CRISPR journal
|May 13, 2025
PubMed
概括

基因疗法提供了一种对状细胞疾病 (SCD) 的有希望的治疗方法,这是一种遗传性血液疾病. 基因编辑的进步正在为新疗法铺平道路,尽管仍然存在挑战.

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