Erythroid Transcription Factor EKLF/KLF1 Mutation Causing Congenital Dyserythropoietic Anemia Type IV in a Patient of Taiwanese Origin: Review of All Reported Cases and Development of a Clinical Diagnostic Paradigm

KLF1 is an erythroid specific transcription factor that is involved in erythroid lineage commitment, globin switching and terminal red blood cell maturation. Various mutations of KLF1 have been identified in humans, which has led to both benign and pathological phenotypes. The E325K mutation, within...

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Dettagli Bibliografici
Pubblicato in:Blood Cells Mol Dis
Autori principali: Jaffray, Julie A., Mitchell, W. Beau, Gnanapragasam, Merlin Nithya, Seshan, Surya V, Guo, Xinhuo, Westhoff, Connie M., Bieker, James J., Manwani, Deepa
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2013
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4560093/
https://ncbi.nlm.nih.gov/pubmed/23522491
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bcmd.2013.02.006
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