Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein

CDA type I is a rare hereditary anemia, characterized by relative reticulocytopenia, and congenital anomalies. It is caused by biallelic mutations in one of the two genes: (i) CDAN1, encoding Codanin-1, which is implicated in nucleosome assembly and disassembly; (ii) C15orf41, which is predicted to...

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Detalhes bibliográficos
Publicado no:Front Physiol
Main Authors: Russo, Roberta, Marra, Roberta, Andolfo, Immacolata, De Rosa, Gianluca, Rosato, Barbara Eleni, Manna, Francesco, Gambale, Antonella, Raia, Maddalena, Unal, Sule, Barella, Susanna, Iolascon, Achille
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2019
Assuntos:
Physiology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6539198/
https://ncbi.nlm.nih.gov/pubmed/31191338
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2019.00621
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