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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Detalles Bibliográficos
Autores principales: Noy-Lotan, Sharon, Dgany, Orly, Marcoux, Nathaly, Atkins, Ayelet, Kupfer, Gary M., Bosques, Linette, Gottschalk, Christine, Steinberg-Shemer, Orna, Motro, Benny, Tamary, Hannah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255688/
https://www.ncbi.nlm.nih.gov/pubmed/34234691
http://dx.doi.org/10.3389/fphys.2021.685242

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255688/
https://www.ncbi.nlm.nih.gov/pubmed/34234691
http://dx.doi.org/10.3389/fphys.2021.685242

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