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UKWNLi005-A
Registration Summary
:
A
P
E
C
GLA-S126G-iPSC
The cell line is
not submitted
yet.
(only basic data is shown)
General
Cell Line
hPSCreg name
UKWNLi005-A
Cite as:
When citing this cell line, please use the hPSCreg name (see
Naming Tool
) and the corresponding Research Resource ID (RRID).
UKWNLi005-A (RRID:CVCL_B5II)
Alternative name(s)
GLA-S126G-iPSC
Cell line type
Human induced pluripotent stem cell (hiPSC)
Similar lines
No similar lines found.
Last update
16th March 2022
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Provider
Generator
Neurologische Klinik (UKWNL)
External Databases
Cellosaurus
CVCL_B5II
Wikidata
Q110433933
General Information
Publications
Breyer M et al. Generation of the induced pluripotent stem cell line UKWNLi005-A derived from a patient with the GLA mutation c.376A > G of unknown pathogenicity in Fabry disease. Stem cell research. 2022 May;61:102747.
Breyer Maximilian et al. In vitro characterization of cells derived from a patient with the GLA variant c.376A>G (p.S126G) highlights a non-pathogenic role in Fabry disease. Molecular Genetics and Metabolism Reports. 2024-03-00.
Klein Alexandra et al. Genetic variants of unknown significance in alpha‐galactosidase A: Cellular delineation from Fabry disease. Journal of Inherited Metabolic Disease. 2024-07-00.
hIPSC Derivation
General
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