A zebrafish model for HAX1-associated congenital neutropenia
Severe congenital neutropenia (CN) is a rare heterogeneous group of diseases, characterized by a granulocytic maturation arrest. Autosomal recessive mutations in the HAX1 gene are frequently detected in affected individuals. However, the precise role of HAX1 during neutrophil differentiation is poo...
Na minha lista:
| Principais autores: | , , , , , |
|---|---|
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Ferrata Storti Foundation
2020-04-01
|
| 叢編: | Haematologica |
| 在線閱讀: | https://haematologica.org/article/view/9727 |
| 標簽: |
沒有標簽, 成為第一個標記此記錄!
|