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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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Bibliografiske detaljer
Udgivet i: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
Format: Artigo
Sprog:Inglês
Udgivet: Frontiers Media S.A. 2021
Fag:
Online adgang: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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