Cystic biliary atresia with paucity of bile ducts and gene mutation in KDM6A: a case report.
Daisuke MasuiSuguru FukahoriTatsuki MizuochiYoriko WatanabeKaori FukuiShinji IshiiNobuyuki SaikusaNaoki HashizumeNaruki HigashidateSaki SakamotoAiko TakatoKoh-Ichiro YoshiuraYoshiaki TanakaMinoru YagiPublished in: Surgical case reports (2019)
Based on the interesting findings of the present case, we hypothesized that KDM6A is associated with hepatic malformations via a connection with the Notch signaling pathway.