OBO ID: DOID:0050590

Citations

(3 total)

Term: severe congenital neutropenia

Linder, M.I., Mizoguchi, Y., Hesse, S., Csaba, G., Tatematsu, M., Łyszkiewicz, M., Zietara, N., Jeske, T., Hastreiter, M., Rohlfs, M., Liu, Y., Grabowski, P., Ahomaa, K., Maier-Begandt, D., Schwestka, M., Pazhakh, V., Isiaku, A., Briones Miranda, B., Blombery, P., Saito, M.K., Rusha, E., Alizadeh, Z., Pourpak, Z., Kobayashi, M., Rezaei, N., Unal, E., Hauck, F., Drukker, M., Walzog, B., Rappsilber, J., Zimmer, R., Lieschke, G.J., Klein, C. (2022) Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes. Blood. 141(6):645-658

Doll, L., Aghaallaei, N., Dick, A.M., Welte, K., Skokowa, J., Bajoghli, B. (2020) A zebrafish model for HAX1-associated congenital neutropenia. Haematologica. 106(5):1311-1320

Pazhakh, V., Clark, S., Keightley, M.C., Lieschke, G.J. (2017) A GCSFR/CSF3R zebrafish mutant models the persistent basal neutrophil deficiency of severe congenital neutropenia. Scientific Reports. 7:44455