Examination of 11 HCC cell lines for β-catenin, AXIN1, and AXIN2 mutations confirmed the previously reported mutations in β-catenin in HepG2 and SNU449 cells and AXIN1 mutations in SNU423 ...

We share a case of a 40-year-old African American woman with a history of Asherman syndrome and asthma who was identified with a rare AXIN2 mutation through her hypodontia and detailed family history.