FIGURE SUMMARY
- Title
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Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes
- Authors
- 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.
- Source
- Full text @ Blood
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Acknowledgments