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Paper Details

Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.
Blood
8
2023
ELANE, HAX1, Human, SRP, SRP-deficiency, SRP19, SRPRA, congenital neutropenia, genetic defects, genetic defects in, human, human induced pluripotent stem cells, neutrophil, neutrophil granulocyte, neutrophil granulocytes, patients, signal recognition particle, signal recognition particle (SRP) genes, zebrafish
Author NameAffiliation
Gergely Csaba
Gergely Csaba
Tim JeskeDr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-Universitat (LMU)
Tim Jeske
Maximilian HastreiterDr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-Universitat (LMU)
Fabian HauckDr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-Universitat (LMU)
Juri RappsilberInstitute of Biotechnology, Technical University of Berlin
Ralf Zimmer
Ralf Zimmer
Christoph KleinDr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-Universitat (LMU)
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Release 1.2