Novel human cellular model of CDA IV enables comprehensive analysis revealing molecular basis of disease phenotype (2023)

First Author: Ferrer-Vicens I

Attributed to: Molecular mechanism by which the E325K mutation of human KLF1 causes a severe dyserythropoietic anemia, utilising a novel model system of RBC disease funded by MRC

No abstract provided

Type: Journal Article/Review

Parent Publication: Blood