最近在遗传性听力损失的基因疗法的临床前和临床进展

Seung Hyun Jang1, Hyeong Gi Song1, Jinsei Jung2

  • 1Department of Pharmacology, Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; Won-Sang Lee Institute for Hearing Loss, Seoul 03722, Republic of Korea.

Molecules and cells
|October 14, 2025
PubMed
概括

基因疗法为遗传性听力损失提供了新的希望,在临床试验中,腺相关病毒载体显示出有前途. 像CRISPR这样的基因组编辑技术为治疗遗传内耳缺陷提供了进一步的潜力.

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