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...
محفوظ في:
| المؤلفون الرئيسيون: | , , , , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Ferrata Storti Foundation
2020-04-01
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| سلاسل: | Haematologica |
| الوصول للمادة أونلاين: | https://haematologica.org/article/view/9727 |
| الوسوم: |
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