Anemia‐associated mutations disrupt the CDIN1 ‐Codanin1 complex in inherited congenital dyserythropoietic anemia I ( CDA ‐I) disease

Congenital dyserythropoietic anemia type I (CDA‐I) is a rare hereditary disease marked by ineffective erythropoiesis, a characteristic spongy heterochromatin structure in erythroblasts, and mutations in the genes CDAN1 and CDIN1 , which encode the proteins Codanin1 and CDIN1. Codanin1 regulates hist...

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Bibliographic Details
Published in:The FEBS journal 2026-01
Main Authors: Stojaspal, Martin, Brom, Tomas, Nečasová, Ivona, Janovič, Tomáš, Veverka, Pavel, Verma, Naina, Uhrík, Lukáš, Hernychova, Lenka, Hofr, Ctirad
Format: Article
Language:English
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