肢体发育
生物
发病机制
细胞凋亡
癌症研究
生物信息学
病理
细胞生物学
基因
遗传学
医学
免疫学
作者
Arielle S. Strasser,Ana S. González-Reiche,Xianxiao Zhou,Braulio Valdebenito‐Maturana,Xiaoqian Ye,Bin Zhang,Meng Wu,Harm van Bakel,Ethylin Wang Jabs
标识
DOI:10.1038/s41467-024-51328-3
摘要
Roberts syndrome (RBS) is an autosomal recessive disorder with profound growth deficiency and limb reduction caused by ESCO2 loss-of-function variants. Here, we elucidate the pathogenesis of limb reduction in an Esco2
科研通智能强力驱动
Strongly Powered by AbleSci AI