Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene

Por Leoyklang, Petcharat, Suphapeetiporn, Kanya, Srichomthong, Chalurmpon, Tongkobpetch, Siraprapa, Fietze, Stefanie, Dorward, Heidi, Cullinane, Andrew R., Gahl, William A., Huizing, Marjan, Shotelersuk, Vorasuk
Publicado em 2013