Borbaran Bravo, N., Doll, L., Deordieva, E., Bräuning, S., Dannenmann, B., ElGamacy, M., Zakharova, V., Lengerke, C., Zeidler,
C., Welte, K., Shcherbina, A., Skokowa, J., & Klimiankou, M. (2023). A New Hereditary
Syndrome with Severe Neutropenia and Neurological Involvement Caused by the Autosomal Recessive COPZ1 Mutation.
HemaSphere: open access journal of the European Hematology Association, 7(Supplement
3):, 180-181. doi:10.1097/01.HS9.0000967624.93623.49.