Recapitulation of erythropoiesis in congenital dyserythropoietic anemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities

The investigation of inherited disorders of erythropoiesis has elucidated many of the principles underlying the production of normal red blood cells and how this is perturbed in human disease. Congenital dyserythropoietic anemia type 1 (CDA-I) is a rare form of anemia caused by mutations in two gene...

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Detalles Bibliográficos
Autores principales: Scott, Caroline, Downes, Damien J., Brown, Jill M., Beagrie, Robert A., Olijnik, Aude-Anais, Gosden, Matthew, Schwessinger, Ron, Fisher, Christopher A., Rose, Anna, Ferguson, David J.P, Johnson, Errin, Hill, Quentin A., Okoli, Steven, Renella, Raffaele, Ryan, Kate, Brand, Marjorie, Hughes, Jim, Roy, Noemi B.A., Higgs, Douglas R., Babbs, Christian, Buckle, Veronica J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Fondazione Ferrata Storti 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561284/
https://www.ncbi.nlm.nih.gov/pubmed/33121234
http://dx.doi.org/10.3324/haematol.2020.260158

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561284/
https://www.ncbi.nlm.nih.gov/pubmed/33121234
http://dx.doi.org/10.3324/haematol.2020.260158

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