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    Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

    Sjaak Philipsen and colleagues report that haploinsufficiency for KLF1 causes hereditary persistence of fetal hemoglobin in a large Maltese family. They further show that KLF1 is a key activator of BCL11A, whi...

    Joseph Borg, Petros Papadopoulos, Marianthi Georgitsi, Laura Gutiérrez in Nature Genetics (2010)