ID   GM09208
AC   CVCL_5U22
SY   MDS3 Fib
DR   CLO; CLO_0010635
DR   Coriell; GM09208
DR   Wikidata; Q54843610
RX   CelloPub=CLPUB00447;
RX   PubMed=24413397;
CC   Derived from site: In situ; Fetal diaphragm, skeletal muscle; UBERON=UBERON_0010084+UBERON_0004495.
CC   Cell type: Fibroblast of skeletal muscle; CL=CL_0011027.
DI   NCIt; C124852; Miller-Dieker syndrome
DI   ORDO; Orphanet_531; Miller-Dieker syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_5U23 ! GM09209
OI   CVCL_5U24 ! GM09210
SX   Male
AG   18FW
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 29-06-23; Version: 10
//
RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//
RX   PubMed=24413397; DOI=10.1038/nature12923; PMCID=PMC4030630;
RA   Bershteyn M., Hayashi Y., Desachy G., Hsiao E.C., Sami S., Tsang K.M.,
RA   Weiss L.A., Kriegstein A.R., Yamanaka S., Wynshaw-Boris A.;
RT   "Cell-autonomous correction of ring chromosomes in human induced
RT   pluripotent stem cells.";
RL   Nature 507:99-103(2014).
//