CPGHi002-A

A P E C

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iPSC Line
hPSCreg name	CPGHi002-A
Cite as:	CPGHi002-A (RRID:CVCL_A1AZ)
iPSC line type	Human induced pluripotent stem cell (hiPSC)
Similar iPSC lines	No similar lines found.
Last update	9th September 2020
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Provider
Generator	Chinese PLA General Hospital (CPGH)
External iPSC Databases
BioSamples	SAMEA7340582
Cellosaurus	CVCL_A1AZ
Wikidata	Q102113716
General iPSC Information
Publications	Gao X et al. Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1B2. Stem cell research. 2020 Oct;48:101986. Gao X et al. Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with heterozygous c.1516 C>T mutation in the ATP6V1B2 gene. Stem cell research. 2021 May;53:102271. Durán-Alonso MB et al. Induced Pluripotent Stem Cells, a Stepping Stone to In Vitro Human Models of Hearing Loss. Cells. 2022 Oct 21;11(20). Amore Greta et al. ATP6V1B2-related disorders featuring Lennox-Gastaut-syndrome: A case-based overview. Brain and Development. 2023-11-00. Ma Tsz Ching Nadine et al. Exploring ATP6V1B2-related disorders: a case report-based literature review. Clinical Dysmorphology. 2026-04-00.
Subclones	CPGHi002-A-1