SDQLCHi017-A

A P E C

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iPSC Line
hPSCreg name	SDQLCHi017-A
Cite as:	SDQLCHi017-A (RRID:CVCL_YK78)
iPSC line type	Human induced pluripotent stem cell (hiPSC)
Similar iPSC lines	No similar lines found.
Last update	10th September 2019
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Provider
Generator	Children’s Hospital affiliated to Shandong University (SDQLCH)
External iPSC Databases
Cellosaurus	CVCL_YK78
Wikidata	Q98129481
General iPSC Information
Publications	Ma Y et al. An integration-free iPSC line (SDQLCHi017-A) derived from a patient with nemaline myopathy-2 disease carrying compound heterozygote mutations in NEB gene. Stem cell research. 2020 Mar;43:101729. Gartz M et al. ACTA1 H40Y mutant iPSC-derived skeletal myocytes display mitochondrial defects in an in vitro model of nemaline myopathy. Experimental cell research. 2023 Mar 15;424(2):113507. Kim Hyun-Jun et al. Keeping your strength up: induced pluripotent stem cell-based approaches for the treatment and investigation of skeletal muscle disorders. All Life. 2023-12-04.