(2012) Congenital Asplenia in Mice and Humans with Mutations in a Pbx/Nkx2-5/p15 Module.
Publication information:
Koss, Bolze, Brendolan, Saggese, Capellini T, Bojilova, Boisson, Prall O, Elliott D, Solloway, et al. (2012) Congenital Asplenia in Mice and Humans with Mutations in a Pbx/Nkx2-5/p15 Module. Developmental Cell. 2012;22:913–26.