在希望和现实之间:通过基于核酸的药物治疗遗传疾病

Virginie Baylot1, Thi Khanh Le2, David Taïeb2

  • 1Aix Marseille Univ, CNRS, CINAM, ERL INSERM U 1326, CERIMED, Marseille, France. virginie.baylot@inserm.fr.

Communications biology
|April 23, 2024
PubMed
概括

基于核酸 (NA) 的疗法为罕见疾病 (RD) 提供了新的希望,彻底改变了治疗方法. 本审查涵盖已批准和正在研究的NA药物,输送系统以及罕见病患者的伦理考虑.

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