ID   GM05112
AC   CVCL_5N08
DR   CLO; CLO_0025379
DR   Coriell; GM05112
DR   Wikidata; Q54838862
RX   PubMed=23665875;
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:2928; DMD; Unexplicit; Ex45del; Zygosity=Hemizygous (Coriell=GM05112).
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_5N09 ! GM05113
SX   Male
AG   13Y
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 19-12-24; Version: 11
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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).
//