OBO ID: DOID:0060485

Citations

(2 total)

Term: Mowat-Wilson syndrome

Ghoumid, J., Drevillon, L., Alavi-Naini, S.M., Bondurand, N., Rio, M., Briand-Suleau, A., Nasser, M., Goodwin, L., Raymond, P., Yanicostas, C., Goossens, M., Lyonnet, S., Mowat, D., Amiel, J., Soussi-Yanicostas, N., and Giurgea, I. (2013) ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild Mowat-Wilson syndrome. Human molecular genetics. 22(13):2652-61

Cui, S., Erlichman, J., Russo, P., Haber, B.A., and Matthews, R.P. (2011) Intrahepatic Biliary Anomalies in a Patient With Mowat-Wilson Syndrome Uncover a Role for the Zinc Finger Homeobox Gene zfhx1b in Vertebrate Biliary Development. Journal of pediatric gastroenterology and nutrition. 52(3):339-344