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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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Бібліографічні деталі
Автори: Beren Karaosmanoglu, M. Alper Kursunel, Duygu Uckan Cetinkaya, Fatma Gumruk, Gunes Esendagli, Sule Unal, Ekim Z. Taskiran
Формат: Artigo
Мова:Inglês
Опубліковано: Frontiers Media S.A. 2021-06-01
Серія:Frontiers in Physiology
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Онлайн доступ:https://www.frontiersin.org/articles/10.3389/fphys.2021.679919/full
Теги: Додати тег
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