Linder, M. I. Et Al. 2023. Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.. Blood , vol.141, no.6 , 645-658.

Linder, M. I., Mizoguchi, Y., Hesse, S., Csaba, G., Tatematsu, M., Łyszkiewicz, M., ... Zietara, N.(2023). Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.. Blood , vol.141, no.6, 645-658.

Linder, Monika Et Al. "Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.," Blood , vol.141, no.6, 645-658, 2023

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, pp.645-658, 2023

Linder, M. I. Et Al. (2023) . "Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.." Blood , vol.141, no.6, pp.645-658.

@article{article, author={Monika I Linder Et Al. }, title={Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.}, journal={Blood}, year=2023, pages={645-658} }