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A novel nonsense RPS26 mutation in a patient with Diamond–Blackfan anemia: a case report

Abstract Background Diamond–Blackfan anemia is a rare congenital disorder characterized by erythroid hypoplasia and is associated with mutations in ribosomal protein genes. This case report describes a novel variant in the RPS26 gene, which, to our knowledge, has not been previously documented. Repo...

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Hlavní autoři: Şule Çalışkan Kamış, Metin Çil, Begül Yağcı, Özlem Anlaş
Médium: Artigo
Jazyk:Inglês
Vydáno: BMC 2024-11-01
Edice:Journal of Medical Case Reports
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On-line přístup:https://doi.org/10.1186/s13256-024-04907-3
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