Nakamura, Yukio; Weidinger, Gilbert; Liang, Jennifer O.; Aquilina-Beck, Allisan; Tamai, Keiko; Moon, Randall T.; Warman, Matthew L.(2007-09-06)
In humans, loss-of-function mutations in the gene encoding Wnt1 inducible signaling pathway protein 3 (WISP3) cause the autosomal-recessive skeletal disorder progressive pseudorheumatoid dysplasia (PPD). However, in mice ...