ID   GM05835
AC   CVCL_5N35
SY   GM5835
DR   CLO; CLO_0024708
DR   Coriell; GM05835
DR   Wikidata; Q54841957
RX   CelloPub=CLPUB00447;
RX   PubMed=10377420;
CC   Karyotypic information: 46,X,t(X;5)(p21.2;q35.3) (PubMed=10377420).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C75482; Duchenne muscular dystrophy
DI   ORDO; Orphanet_98896; Duchenne muscular dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   10Y
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 29-06-23; Version: 11
//
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=10377420; DOI=10.1073/pnas.96.13.7364; PMCID=PMC22091;
RA   Carrel L., Willard H.F.;
RT   "Heterogeneous gene expression from the inactive X chromosome: an
RT   X-linked gene that escapes X inactivation in some human cell lines but
RT   is inactivated in others.";
RL   Proc. Natl. Acad. Sci. U.S.A. 96:7364-7369(1999).
//