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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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Detalles Bibliográficos
Autores principales:	Doll, Larissa, Aghaallaei, Narges, Dick, Advaita M., Welte, Karl, Skokowa, Julia, Bajoghli, Baubak
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Fondazione Ferrata Storti 2020
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094079/ https://www.ncbi.nlm.nih.gov/pubmed/32327498 http://dx.doi.org/10.3324/haematol.2019.240200

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