Marko Schwestka
1PUBLICATIONS
13CO-AUTHORS
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Publications (1)
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|Oct 12, 2022
Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.Monika I Linder, Yoko Mizoguchi, Sebastian Hesse
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Sebastian Hesse
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Tim Jeske
1 joint publications
Daniela Maier-Begandt
1 joint publications
Abdulsalam I Isiaku
1 joint publications
Brenda Briones Miranda
1 joint publications
Zahra Alizadeh
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Zahra Pourpak
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Nima Rezaei
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Fabian Hauck
1 joint publications
Micha Drukker
