Deficiency of ribosomal protein S26, which is mutated in a subset of patients with Diamond Blackfan anemia, impairs erythroid differentiation

Introduction: Diamond Blackfan anemia (DBA) is a rare congenital disease characterized by defective maturation of the erythroid progenitors in the bone marrow, for which treatment involves steroids, chronic transfusions, or hematopoietic stem cells transplantation. Diamond Blackfan anemia is caused...

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Detalles Bibliográficos
Autores principales: Piantanida, Noemy, La Vecchia, Marta, Sculco, Marika, Talmon, Maria, Palattella, Gioele, Kurita, Ryo, Nakamura, Yukio, Ronchi, Antonella Ellena, Dianzani, Irma, Ellis, Steven R., Fresu, Luigia Grazia, Aspesi, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790993/
https://www.ncbi.nlm.nih.gov/pubmed/36579335
http://dx.doi.org/10.3389/fgene.2022.1045236

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790993/
https://www.ncbi.nlm.nih.gov/pubmed/36579335
http://dx.doi.org/10.3389/fgene.2022.1045236

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