A novel human cellular model of CDA IV enables comprehensive analysis revealing the molecular basis of the 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

PubMed Identifier: 37084386

Type: Journal Article/Review

Volume: 141

Parent Publication: Blood

Issue: 25

ISSN: 0006-4971