Cdan1 Is Essential for Primitive Erythropoiesis

Congenital dyserythropoietic anemia type I (CDA I) is an autosomal recessive disease characterized by moderate to severe macrocytic anemia and pathognomonic morphologic abnormalities of the erythroid precursors, including spongy heterochromatin. The disease is mainly caused by mutations in CDAN1 (en...

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Detalhes bibliográficos
Publicado no:Front Physiol
Main Authors: Noy-Lotan, Sharon, Dgany, Orly, Marcoux, Nathaly, Atkins, Ayelet, Kupfer, Gary M., Bosques, Linette, Gottschalk, Christine, Steinberg-Shemer, Orna, Motro, Benny, Tamary, Hannah
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2021
Assuntos:
Physiology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8255688/
https://ncbi.nlm.nih.gov/pubmed/34234691
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2021.685242
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