ID   CIPi001-A
AC   CVCL_B3S5
SY   iPSC-16p11.2 deletion
DR   BioSamples; SAMEA10271033
DR   hPSCreg; CIPi001-A
DR   Wikidata; Q110432723
RX   PubMed=34995844;
CC   From: Children's Hospital of Capital Institute of Pediatrics; Beijing; China.
CC   Population: Chinese.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C183308; Benign familial infantile seizures
DI   NCIt; C120408; Chromosome 16p11.2 deletion syndrome
DI   ORDO; Orphanet_306; Benign familial infantile epilepsy
DI   ORDO; Orphanet_261197; Proximal 16p11.2 microdeletion syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   4Y3M
CA   Induced pluripotent stem cell
DT   Created: 16-12-21; Last updated: 29-06-23; Version: 4
//
RX   PubMed=34995844; DOI=10.1016/j.scr.2021.102634;
RA   Ji X.-N., Gao Y.-Y., Zhang P.-P., Jin Z.-Q., Zhang Y., Yang M.-N.,
RA   Zhang X., Chen Q.;
RT   "Generation of a human iPSC line CIPi001-A from a benign familial
RT   infantile epilepsy patient related 16p11.2 deletion.";
RL   Stem Cell Res. 59:102634-102634(2022).
//