Kathleen A. Williamson

1. Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects
   2014/01/23 by Kathleen A. Williamson, Kathleen A. Williamson, Joe Rainger +25 · 28 citations
   Biochemistry, Genetics and Molecular Biology · #Hippo pathway signaling and YAP/TAZ