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Human genetic defects in SRP19 and SRPRA cause severe conge..:
Linder, Monika I.
;
Mizoguchi, Yoko
;
Hesse, Sebastian
...
Blood. 141 (2023) 6 - p. 645-658 , 2023
Link:
https://doi.org/10.1182/blood.2022016783
RT Journal T1
Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes
UL https://suche.suub.uni-bremen.de/peid=cr-10.1182_blood.2022016783&Exemplar=1&LAN=DE A1 Linder, Monika I. A1 Mizoguchi, Yoko A1 Hesse, Sebastian A1 Csaba, Gergely A1 Tatematsu, Megumi A1 Łyszkiewicz, Marcin A1 Ziȩtara, Natalia A1 Jeske, Tim A1 Hastreiter, Maximilian A1 Rohlfs, Meino A1 Liu, Yanshan A1 Grabowski, Piotr A1 Ahomaa, Kaarin A1 Maier-Begandt, Daniela A1 Schwestka, Marko A1 Pazhakh, Vahid A1 Isiaku, Abdulsalam I. A1 Briones Miranda, Brenda A1 Blombery, Piers A1 Saito, Megumu K. A1 Rusha, Ejona A1 Alizadeh, Zahra A1 Pourpak, Zahra A1 Kobayashi, Masao A1 Rezaei, Nima A1 Unal, Ekrem A1 Hauck, Fabian A1 Drukker, Micha A1 Walzog, Barbara A1 Rappsilber, Juri PB American Society of Hematology YR 2023 SN 0006-4971 SN 1528-0020 JF Blood VO 141 IS 6 SP 645 OP 658 LK http://dx.doi.org/https://doi.org/10.1182/blood.2022016783 DO https://doi.org/10.1182/blood.2022016783 SF ELIB - SuUB Bremen
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