ID   CBRCULi018-A
AC   CVCL_D6FW
SY   91-2032-7; 91-2032 clone 7
DR   BioSamples; SAMEA115098117
DR   hPSCreg; CBRCULi018-A
DR   Wikidata; Q127380405
RX   PubMed=38490135;
CC   From: CERVO Brain Research Centre, Universite Laval; Quebec; Canada.
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; 2933; DMPK; Repeat_expansion; c.*224CTG[~2000] (c.*224CTG[(51_?)]); ClinVar=VCV000005049; Zygosity=Heterozygous (PubMed=38232626).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C84679; Dystrophia myotonica 1
DI   ORDO; Orphanet_273; Steinert myotonic dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   58Y
CA   Induced pluripotent stem cell
DT   Created: 02-05-24; Last updated: 10-09-24; Version: 2
//
RX   PubMed=38490135; DOI=10.1016/j.scr.2024.103375;
RA   Pierre M., Jauvin D., Puymirat J., Boutjdir M., Chahine M.;
RT   "Generation of three myotonic dystrophy type 1 patient iPSC lines
RT   (CBRCULi018-A, CBRCULi019-A, CBRCULi020-A) derived from
RT   lymphoblastoid cell lines for disease modelling and therapeutic
RT   research.";
RL   Stem Cell Res. 76:103375-103375(2024).
//