Proerythroblast Cells of Diamond-Blackfan Anemia Patients With RPS19 and CECR1 Mutations Have Similar Transcriptomic Signature

Diamond Blackfan Anemia (DBA) is an inherited bone marrow (BM) failure syndrome, characterized by a paucity of erythroid differentiation. DBA is mainly caused by the mutations in ribosomal protein genes, hence classified as ribosomopathy. However, in approximately 30% of patients, the molecular etio...

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Detalles Bibliográficos
Autores principales: Karaosmanoglu, Beren, Kursunel, M. Alper, Uckan Cetinkaya, Duygu, Gumruk, Fatma, Esendagli, Gunes, Unal, Sule, Taskiran, Ekim Z.
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/PMC8226250/
https://www.ncbi.nlm.nih.gov/pubmed/34177624
http://dx.doi.org/10.3389/fphys.2021.679919

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8226250/
https://www.ncbi.nlm.nih.gov/pubmed/34177624
http://dx.doi.org/10.3389/fphys.2021.679919

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