ID   UMGi046-A
AC   CVCL_A4JL
SY   iBrs1
DR   hPSCreg; UMGi046-A
DR   Wikidata; Q105511508
RX   PubMed=27485484;
WW   Provider; UMCG; -; https://sfb1002.med.uni-goettingen.de/production/cellmodel/cell-line/view?tab=internal&line=66
CC   From: University Medical Center Goettingen; Goettingen; Germany.
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C142891; Brugada syndrome
DI   ORDO; Orphanet_130; Brugada syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   49Y
CA   Induced pluripotent stem cell
DT   Created: 12-01-21; Last updated: 10-04-25; Version: 6
//
RX   PubMed=27485484; DOI=10.1038/srep30967; PMCID=PMC4971529;
RA   Veerman C.C., Mengarelli I., Guan K.-M., Stauske M., Barc J., Tan H.L.,
RA   Wilde A.A.M., Verkerk A.O., Bezzina C.R.;
RT   "hiPSC-derived cardiomyocytes from Brugada syndrome patients without
RT   identified mutations do not exhibit clear cellular
RT   electrophysiological abnormalities.";
RL   Sci. Rep. 6:30967-30967(2016).
//