ID   ASC clone 23
AC   CVCL_D6RQ
SY   ASC23
RX   PubMed=30089820;
CC   From: Department of Functional Genomics - Human Molecular Genetics, University Medicine Greifswald; Greifswald; Germany.
CC   Population: Palestinian.
CC   Omics: Transcriptomics; RNAseq.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   Children
CA   Induced pluripotent stem cell
DT   Created: 10-09-24; Last updated: 10-04-25; Version: 2
//
RX   PubMed=30089820; DOI=10.1038/s41431-018-0220-5; PMCID=PMC6244410;
RA   van Diepen L., Buettner F.F.R., Hoffmann D., Thiesler C.T.,
RA   von Bohlen und Halbach O., von Bohlen und Halbach V., Jensen L.R.,
RA   Steinemann D., Edvardson S., Elpeleg O., Schambach A.,
RA   Gerardy-Schahn R., Kuss A.W.;
RT   "A patient-specific induced pluripotent stem cell model for West
RT   syndrome caused by ST3GAL3 deficiency.";
RL   Eur. J. Hum. Genet. 26:1773-1783(2018).
//