ID   UIi001-A
AC   CVCL_B5RX
SY   SCZ019-A; SCZ019
DR   hPSCreg; UIi001-A
DR   Wikidata; Q112041881
RX   PubMed=34953327;
CC   From: University of Iowa; Iowa City; USA.
CC   Population: Caucasian.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C120408; Chromosome 16p11.2 deletion syndrome
DI   NCIt; C3362; Schizophrenia
DI   ORDO; Orphanet_261197; Proximal 16p11.2 microdeletion syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   33Y
CA   Induced pluripotent stem cell
DT   Created: 17-03-22; Last updated: 29-06-23; Version: 4
//
RX   PubMed=34953327; DOI=10.1016/j.scr.2021.102636;
RA   Madencioglu D.A., Kruth K., Shin M., Andreasen N.C., Wassink T.H.,
RA   Williams A.J.;
RT   "Generation of a human induced pluripotent stem cell line from a
RT   patient diagnosed with schizophrenia carrying a 16p11.2 deletion.";
RL   Stem Cell Res. 59:102636-102636(2022).
//