AARS2 R199C mutation induces lactylation-driven premature ovarian insufficiency phenotypes partially reversible by SIRT3.

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DOI:10.1093/reprod/xaag035
作者：Hai-Hui Zhang, Zhi-Ling Zhang, Wei Xu
文献类型：期刊论文
补充材料：只需要正文

Oxford University Press

Abstract：Premature ovarian insufficiency (POI) often arises from genetic causes, yet the pathogenic consequences of many variants remain undefined. The AARS2 R199C mutation has been repeatedly report

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