ID   PS-iPS2
AC   CVCL_CW47
DR   Wikidata; Q54948407
RX   PubMed=23400930;
CC   Sequence variation: Mutation; HGNC; HGNC:Group_1972; MT-@; Unexplicit; m.10949del2501; Zygosity=Heteroplasmic (PubMed=23400930).
CC   Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
DI   NCIt; C115326; Pearson syndrome
DI   ORDO; Orphanet_699; Pearson syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_CW46 ! PS-iPS1
OI   CVCL_CW48 ! PS-iPS3
SX   Female
AG   3Y
CA   Induced pluripotent stem cell
DT   Created: 13-07-16; Last updated: 19-12-24; Version: 11
//
RX   PubMed=23400930; DOI=10.1002/stem.1354; PMCID=PMC3692613;
RA   Cherry A.B.C., Gagne K.E., McLoughlin E.M., Baccei A., Gorman B.,
RA   Hartung O., Miller J.D., Zhang J., Zon R.L., Ince T.A., Neufeld E.J.,
RA   Lerou P.H., Fleming M.D., Daley G.Q., Agarwal S.;
RT   "Induced pluripotent stem cells with a mitochondrial DNA deletion.";
RL   Stem Cells 31:1287-1297(2013).
//