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...
Gardado en:
| Principais autores: | , , , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Ferrata Storti Foundation
2020-04-01
|
| Series: | Haematologica |
| Acceso en liña: | https://haematologica.org/article/view/9727 |
| Tags: |
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|