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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Vydáno v:Front Physiol
Hlavní autoři: Noy-Lotan, Sharon, Dgany, Orly, Marcoux, Nathaly, Atkins, Ayelet, Kupfer, Gary M., Bosques, Linette, Gottschalk, Christine, Steinberg-Shemer, Orna, Motro, Benny, Tamary, Hannah
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2021
Témata:
Physiology
On-line přístup: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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