ID   IBBISTi004-B
AC   CVCL_B7GT
SY   iPSC AS-GB clone 20; AS-GB clone 20
DR   BioSamples; SAMEA13019138
DR   hPSCreg; IBBISTi004-B
DR   Wikidata; Q112929810
RX   PubMed=35339881;
CC   From: Simao Jose Teixeira da Rocha; Porto Salvo; Portugal.
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C75462; Angelman syndrome
DI   ORDO; Orphanet_72; Angelman syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_B7GS ! IBBISTi004-A
OI   CVCL_B7GU ! IBBISTi004-C
SX   Female
AG   3Y
CA   Induced pluripotent stem cell
DT   Created: 23-06-22; Last updated: 30-01-24; Version: 5
//
RX   PubMed=35339881; DOI=10.1016/j.scr.2022.102757;
RA   Maranga C., Pereira C.A., Raposo A.C., Vieira A., Duarte S.,
RA   Bekman E.P., Milagre I., da Rocha S.J.T.;
RT   "Generation and characterization of induced pluripotent stem cell line
RT   (IBBISTi004-A) from an Angelman syndrome patient carrying a class II
RT   deletion of the maternal chromosome 15q11.2-q13.";
RL   Stem Cell Res. 61:102757-102757(2022).
//