ID   CHOPi008-C
AC   CVCL_C1NW
SY   DS145.T21.G1
DR   BioSamples; SAMEA111510099
DR   hPSCreg; CHOPi008-C
DR   Wikidata; Q114310962
RX   PubMed=37084616;
CC   From: Children's Hospital of Philadelphia; Philadelphia; USA.
CC   Population: Caucasian.
CC   Karyotypic information: 47,XY,+21 (PubMed=37084616).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C2993; Down syndrome
DI   NCIt; C82339; Transient abnormal myelopoiesis associated with Down syndrome
DI   ORDO; Orphanet_870; Down syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_C1NU ! CHOPi008-A
OI   CVCL_C1NV ! CHOPi008-B
SX   Male
AG   8D
CA   Induced pluripotent stem cell
DT   Created: 22-09-22; Last updated: 05-10-23; Version: 4
//
RX   PubMed=37084616; DOI=10.1016/j.scr.2023.103098; PMCID=PMC10576909;
RA   Takasaki, Kaoru
RA   Kumar, Sara S.
RA   Gagne, Alyssa L.
RA   French, Deborah L.
RA   Chou, Stella T.
RT   "Generation of 2 isogenic clones from a patient with trisomy 21 and a
RT   GATA1 mutation.";
RL   Stem Cell Res. 69:103098-103098(2023).
//