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

Author(s):
Natiq, A.; Lysy, P.A.; Gillemans, N.; Schaap, R.; Sefiani, A.; Amzazi, S.; El-Alaoui, S.C.; Cantu, I.; Banjanin, B.; Lom, K. van; Harteveld, C.L.; Philipsen, S.
Published
2017
Publication type
Article / Letter to editor
Date issued
2017-01-31
Language
English
Is part of
American Journal of Hematology (2017), Vol. 92, no. 1, p. E2-E3
hdl
1887/115959
doi
10.1002/ajh.24574