ID   GM11025
AC   CVCL_1N68
DR   CLO; CLO_0023296
DR   Coriell; GM11025
DR   Wikidata; Q54844806
RX   CelloPub=CLPUB00447;
RX   PubMed=8103757;
CC   Population: Caucasian.
CC   Karyotypic information: 46,X,t(X;4)(Xqter->Xp21::4q35->4qter;4pter->4q35::Xp21->Xpter) (Coriell=GM11025).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C75482; Duchenne muscular dystrophy
DI   ORDO; Orphanet_98896; Duchenne muscular dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   5Y
CA   Transformed cell line
DT   Created: 08-07-15; Last updated: 29-06-23; Version: 12
//
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=8103757; DOI=10.1007/BF00219692;
RA   Wijmenga C., Winokur S.T., Padberg G.W., Skraastad M.I., Altherr M.R.,
RA   Wasmuth J.J., Murray J.C., Hofker M.H., Frants R.R.;
RT   "The human skeletal muscle adenine nucleotide translocator gene maps
RT   to chromosome 4q35 in the region of the facioscapulohumeral muscular
RT   dystrophy locus.";
RL   Hum. Genet. 92:198-203(1993).
//