ID   UUIGPi004-A
AC   CVCL_WT81
SY   UUIGPi004A; UUIGPi04; MW2; MWS26B
DR   hPSCreg; UUIGPi004-A
RX   PubMed=31376723;
CC   From: Department of Immunology, Genetics and Pathology, Uppsala University; Uppsala; Sweden.
CC   Sequence variation: Heterozygous for ZEB2 p.Arg343Ter (c.1027C>T) (PubMed=31376723).
DI   NCIt; C74999; Mowat-Wilson syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens
SX   Female
AG   6Y
CA   Induced pluripotent stem cell
DT   Created: 05-07-19; Last updated: 06-09-19; Version: 2
//
RX   PubMed=31376723; DOI=10.1016/j.scr.2019.101518;
RA   Schuster J., Sobol M., Fatima A., Khalfallah A., Laan L.,
RA   Anderlid B.-M., Nordgren A., Dahl N.;
RT   "Mowat-Wilson syndrome: Generation of two human iPS cell lines
RT   (UUIGPi004A and UUIGPi005A) from siblings with a truncating ZEB2 gene
RT   variant.";
RL   Stem Cell Res. 39:101518-101518(2019).
//