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Genetic disarray follows mutant KLF1-E325K expression in a congenital dyserythropoietic anemia patient
Congenital dyserythropoietic anemia type IV is caused by a heterozygous mutation, Glu325Lys (E325K), in the KLF1 transcription factor. Molecular characteristics of this disease have not been clarified, partly due to its rarity. We expanded erythroid cells from a patient’s peripheral blood and analyz...
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| Publicado no: | Haematologica |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Ferrata Storti Foundation
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6959163/ https://ncbi.nlm.nih.gov/pubmed/30872368 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2018.209858 |
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