ID   UPSFRi011-A
AC   CVCL_QX70
SY   PB38
DR   hPSCreg; UPSFRi011-A
DR   Wikidata; Q54991785
RX   PubMed=29034880;
CC   From: Universite Paris-Sud 11; Paris; France.
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; 1100; BRCA1; Unexplicit; Ex17del; Zygosity=Heterozygous (PubMed=29034880).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C36100; BRCA1-associated hereditary breast and ovarian cancer syndrome
DI   ORDO; Orphanet_145; Hereditary breast and ovarian cancer syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   56Y
CA   Induced pluripotent stem cell
DT   Created: 15-11-17; Last updated: 05-10-23; Version: 9
//
RX   PubMed=29034880; DOI=10.1016/j.scr.2017.09.003;
RA   Griscelli F., Oudrhiri N., Feraud O., Divers D., Portier L.,
RA   Turhan A.G., Bennaceur-Griscelli A.;
RT   "Generation of induced pluripotent stem cell (iPSC) line from a
RT   patient with triple negative breast cancer with hereditary exon 17
RT   deletion of BRCA1 gene.";
RL   Stem Cell Res. 24:135-138(2017).
//