新兴的,新型基因调节疗法用于西氨基酸心肌病变

Song Peng Ang1, Jia Ee Chia2, Debabrata Mukherjee2,3

  • 1Department of Medicine, Rutgers Health/Community Medical Center, Toms River, NJ, USA. spa45@rutgers.edu.

Heart failure reviews
|March 8, 2025
PubMed
概括

像siRNA,ASO和CRISPR-Cas9这样的新型基因调节疗法通过降低TTR蛋白的产生来治疗跨甲基氨基酸心肌病 (ATTR-CM) 的前景有望,这提供了超越当前稳定剂的新希望.