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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

Abstract

No abstract provided

Bibliographic Information

Publication URI: https://ashpublications.org/blood/article/141/25/3039/495423/A-novel-human-cellular-model-of-CDA-IV-enables

Type: Journal Article/Review

Volume: 141

Parent Publication: Blood

Issue: 25