ID   GM05169
AC   CVCL_L752
DR   CLO; CLO_0025274
DR   Coriell; GM05169
DR   Wikidata; Q54838906
RX   PubMed=23665875;
CC   Sequence variation: Mutation; HGNC; HGNC:2928; DMD; Unexplicit; Ex4-43del; Zygosity=Hemizygous (Coriell=GM05169).
CC   Omics: CNV analysis.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C75482; Duchenne muscular dystrophy
DI   ORDO; Orphanet_98896; Duchenne muscular dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_L753 ! GM05170
SX   Male
AG   9Y
CA   Finite cell line
DT   Created: 06-05-13; Last updated: 19-12-24; Version: 15
//
RX   PubMed=23665875; DOI=10.1534/g3.113.006577; PMCID=PMC3704242;
RA   Tang Z.-Y., Berlin D.S., Toji L.H., Toruner G.A., Beiswanger C.M.,
RA   Kulkarni S., Martin C.L., Emanuel B.S., Christman M., Gerry N.P.;
RT   "A dynamic database of microarray-characterized cell lines with
RT   various cytogenetic and genomic backgrounds.";
RL   G3 (Bethesda) 3:1143-1149(2013).
//