Hemoglobin switching in mice carrying the Klf1Nan variant
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DOI: 10.3324/haematol.2019.239830
Abstract: Haploinsufficiency for transcription factor KLF1 causes a variety of human erythroid phenotypes, such as the In(Lu) blood type, increased HbA2 levels, and hereditary persistence of fetal hemoglobin. Severe dominant congenital dyserythropoietic anemia IV (CDA-IV) (OMIM… read more here.
Keywords: klf1nan; hemoglobin; klf1; klf1wt nan ... See more keywords