Axin2 coupled excessive Wnt‐glycolysis signaling mediates social defect in autism spectrum disorders by Mengmeng Wang, Panpan Xian, Weian Zheng, Zhenzhen Li, Andi Chen, Haoxiang Xiao, Chao Xu, Fei Wang, Honghui Mao, Han Meng, Youyi Zhao, Ceng Luo, Yazhou Wang, Shengxi Wu

Subjects: “…Axin2…”
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Identification and Functional Analysis of Novel Mutations in AXIN2 and LRP6 Linked With Non‐Syndromic Tooth Agenesis by Wendi Luo, Haitang Yue, Guangtai Song, Jing Cheng, Miao He

Subjects: “…AXIN2…”
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A rare deleterious missense mutation in the AXIN2 gene in Chinese women with polycystic ovary syndrome by Ying Zhang, Yu Chen, Fa-Ying Liu, Jing-Wen Fu, Xian-Xian Liu, Jun Tan, Ou-Ping Huang, Yang Zou

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