Characterization of the interactions between Codanin-1 and C15Orf41, two proteins implicated in congenital dyserythropoietic anemia type I disease

BACKGROUND: Congenital dyserythropoietic anemia type I (CDA I), is an autosomal recessive disease with macrocytic anemia in which erythroid precursors in the bone marrow exhibit pathognomonic abnormalities including spongy heterochromatin and chromatin bridges. We have shown previously that the gene...

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Detalles Bibliográficos
Autores principales: Swickley, Grace, Bloch, Yehoshua, Malka, Lidor, Meiri, Adi, Noy-Lotan, Sharon, Yanai, Amiel, Tamary, Hannah, Motro, Benny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092493/
https://www.ncbi.nlm.nih.gov/pubmed/32293259
http://dx.doi.org/10.1186/s12860-020-00258-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092493/
https://www.ncbi.nlm.nih.gov/pubmed/32293259
http://dx.doi.org/10.1186/s12860-020-00258-1

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