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A zebrafish model for HAX1-associated congenital neutropenia
Severe congenital neutropenia is a rare heterogeneous group of diseases, characterized by an arrest of granulocyte maturation. Autosomal recessive mutations in the HAX1 gene are frequently detected in affected individuals. However, the precise role of HAX1 during neutrophil differentiation is poorly...
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| Gepubliceerd in: | Haematologica |
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| Hoofdauteurs: | , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Fondazione Ferrata Storti
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8094079/ https://ncbi.nlm.nih.gov/pubmed/32327498 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2019.240200 |
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