Berna Seker Yilmaz1, Paul Gissen1,2,3

  • 1Genetics and Genomic Medicine Department, Great Ormond Street Institute of Child Health, University College London, London WC1N 1EH, UK.

Biomedicines
|August 26, 2023
PubMed
概括

甲基因转糖酶缺乏症 (OTCD) 基因疗法在治疗这种罕见的尿素循环障碍方面表现有前途. 本综述探讨了用于临床翻译的AAV基因添加,mRNA疗法和基因组编辑方法.

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