Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.

MLA

Linder, Monika I., et al. “Human Genetic Defects in SRP19 and SRPRA Cause Severe Congenital Neutropenia with Distinctive Proteome Changes.” Blood, vol. 141, no. 6, Feb. 2023, pp. 645–58. EBSCOhost, https://doi.org/10.1182/blood.2022016783.

APA

Linder, M. I., Mizoguchi, Y., Hesse, S., Csaba, G., Tatematsu, M., Łyszkiewicz, M., Ziȩtara, N., Jeske, T., Hastreiter, M., Rohlfs, M., Liu, Y., Grabowski, P., Ahomaa, K., Maier-Begandt, D., Schwestka, M., Pazhakh, V., Isiaku, A. I., Briones Miranda, B., Blombery, P., … Klein, C. (2023). Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes. Blood, 141(6), 645–658. https://doi.org/10.1182/blood.2022016783

Chicago

Linder, Monika I, Yoko Mizoguchi, Sebastian Hesse, Gergely Csaba, Megumi Tatematsu, Marcin Łyszkiewicz, Natalia Ziȩtara, et al. 2023. “Human Genetic Defects in SRP19 and SRPRA Cause Severe Congenital Neutropenia with Distinctive Proteome Changes.” Blood 141 (6): 645–58. doi:10.1182/blood.2022016783.