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Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2-p13.12/13 deletion.

Abdelhafid NatiqPhilippe A LysyNynke GillemansRianne SchaapAbdelaziz SefianiSaaid AmzaziSiham Chafai El-AlaouiIleana CantúBella BanjaninKirsten van LomCornelis L HarteveldSjaak Philipsen
Published in: American journal of hematology (2016)
Keyphrases
  • transcription factor
  • red blood cell