Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression. (Blood, 2014)

(untitled) - Viprakasit, V; Ekwattanakit, S; Riolueang, S; Chalaow, N; Fisher, C; Lower, K; Kanno, H; Tachavanich, K; Bejrachandra, S; Saipin, J; Juntharaniyom, M; Sanpakit, K; et al.