Systemic mRNA therapy for the treatment of Fabry disease: Preclinical studies in GLA-deficient mice and rats, and wild-typenon-human primates

MOLECULAR GENETICS AND METABOLISM(2018)

引用 0|浏览16
暂无评分
关键词
fabry disease,systemic mrna therapy,gla-deficient,wild-typenon-human
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要