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1 research outputs found
Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes
Author
Ahomaa Kaarin
Alizadeh Zahra
+31 more
Blombery Piers
Briones Miranda Brenda
Csaba Gergely
Drukker Micha
Grabowski Piotr
Hastreiter Maximilian
Hauck Fabian
Hesse Sebastian
Isiaku Abdulsalam
Jeske Tim
Klein Christoph
Kobayashi Masao
Lieschke Graham J.
Linder Monika I.
Liu Yanshan
Maier-Begandt Daniela
Mizoguchi Yoko
Pazhakh Vahid
Pourpak Zahra
Rappsilber Juri
Rezaei Nima
Rohlfs Meino
Rusha Ejona
Saito Megumu K
Schwestka Marko
Tatematsu Megumi
Unal Ekrem
Walzog Barbara
Zietara Natalia
Zimmer Ralf
Łyszkiewicz Marcin
Publication venue
'American Society of Hematology'
Publication date
11/10/2022
Field of study
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Edinburgh Research Explorer
Erciyes University - AVESIS