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@MISC{Stein:279498,
author = {Stein, Frank and Deleidi, Michela},
title = {{D}ataset: {GBA}1 interactome for understanding
pathological mechanisms},
publisher = {PRoteomics IDEntifications Database},
reportid = {DZNE-2025-00825},
year = {2023},
abstract = {Compound heterozygous or homozygous GBA1 mutations lead to
Gaucher disease. Furthermore, GBA1 mutations are the most
frequent risk factor for Parkinson's disease. To get a
better understanding of the pathological mechanisms, we
generated inducible V5-Flag-Tag, V5-Flag-tagged WT, E326K
and L444P mutant Flp-Inâ„¢T-RExâ„¢-HEK293 and
performed interatomic analysis.},
cin = {AG Deleidi},
cid = {I:(DE-2719)1210011},
pnm = {352 - Disease Mechanisms (POF4-352)},
pid = {G:(DE-HGF)POF4-352},
typ = {PUB:(DE-HGF)32},
url = {https://pub.dzne.de/record/279498},
}