Article Versions Notes

Jurk K, Adenaeuer A, Sollfrank S, Groß K, Häuser F, Czwalinna A, Erkel J, Fritsch N, Marandiuc D, Schaller M, et al. Novel GATA1 Variant Causing a Bleeding Phenotype Associated with Combined Platelet α-/δ-Storage Pool Deficiency and Mild Dyserythropoiesis Modified by a SLC4A1 Variant. Cells. 2022; 11(19):3071. https://doi.org/10.3390/cells11193071

Jurk, Kerstin, Anke Adenaeuer, Stefanie Sollfrank, Kathrin Groß, Friederike Häuser, Andreas Czwalinna, Josef Erkel, Nele Fritsch, Dana Marandiuc, Martin Schaller, and et al. 2022. "Novel GATA1 Variant Causing a Bleeding Phenotype Associated with Combined Platelet α-/δ-Storage Pool Deficiency and Mild Dyserythropoiesis Modified by a SLC4A1 Variant" Cells 11, no. 19: 3071. https://doi.org/10.3390/cells11193071

Jurk, K., Adenaeuer, A., Sollfrank, S., Groß, K., Häuser, F., Czwalinna, A., Erkel, J., Fritsch, N., Marandiuc, D., Schaller, M., Lackner, K. J., Rossmann, H., & Bergmann, F. (2022). Novel GATA1 Variant Causing a Bleeding Phenotype Associated with Combined Platelet α-/δ-Storage Pool Deficiency and Mild Dyserythropoiesis Modified by a SLC4A1 Variant. Cells, 11(19), 3071. https://doi.org/10.3390/cells11193071