ID   GM03783
AC   CVCL_5M86
SY   GM 3783; GM3783
DR   CLO; CLO_0015596
DR   BioSample; SAMN00808531
DR   Coriell; GM03783
DR   Wikidata; Q54838233
RX   CelloPub=CLPUB00447;
RX   PubMed=6088703;
RX   PubMed=6574472;
CC   Population: Caucasian; Iberian.
CC   Sequence variation: Mutation; HGNC; HGNC:2928; DMD; Unexplicit; Ex3-17del; Zygosity=Hemizygous (Coriell=GM03783).
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)
OI   CVCL_5M85 ! GM03782
SX   Male
AG   10Y
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 19-12-24; Version: 16
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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=6088703; DOI=10.1016/0022-510x(84)90174-6;
RA   Wright P.S., McKinney E., Berry S., Evers A., Kent C.M.;
RT   "A functional membrane repair system in Duchenne muscular dystrophy
RT   fibroblasts.";
RL   J. Neurol. Sci. 64:259-264(1984).
//
RX   PubMed=6574472; DOI=10.1073/pnas.80.10.3086; PMCID=PMC393979;
RA   Kent C.M.;
RT   "Increased rate of cell-substratum detachment of fibroblasts from
RT   patients with Duchenne muscular dystrophy.";
RL   Proc. Natl. Acad. Sci. U.S.A. 80:3086-3090(1983).
//