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

Frayne, Jan (Principal Investigator)

School of Biochemistry

Status	Finished
Effective start/end date	1/05/18 → 5/04/22

1 Article (Academic Journal)

Loss of ATG5 in Humans Causes Syndromic Congenital Dyserythropoietic Anemia with Impaired Mitophagy in Late Stages of Terminal Erythropoiesis
Ntoumaziou, A., Nguyen, D., Elgammal, Y., Husami, A., Zhang, W., Weaver, K. D., Kasten, J. L., Grier, D. D., Zheng, Y., Lutzko, C., Risinger, M., Frayne, J., Seu, K. & Kalfa, T. A., 6 Dec 2024, In: Blood. 144, Supplement 1, p. 1084-1084 1 p.
Research output: Contribution to journal › Article (Academic Journal) › peer-review

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