ID   DMDCl2
AC   CVCL_6B26
DR   Wikidata; Q54831289
RX   PubMed=22040608;
CC   Sequence variation: Mutation; HGNC; HGNC:2928; DMD; Unexplicit; Ex48-50del; Zygosity=Hemizygous (PubMed=22040608).
CC   Genetic integration: Method=Transduction; Gene=HGNC; HGNC:11730; TERT.
CC   Genetic integration: Method=Transduction; Gene=MGI; MGI:88357; Cdk4.
CC   Genetic integration: Method=Transduction; Gene=UniProtKB; P13249; S.alboniger pac (PuroR).
CC   Genetic integration: Method=Transduction; Gene=UniProtKB; P00552; Transposon Tn5 neo.
CC   Derived from site: In situ; Thigh, quadriceps skeletal muscle; UBERON=UBERON_0004498.
CC   Cell type: Myoblast; CL=CL_0000056.
DI   NCIt; C75482; Duchenne muscular dystrophy
DI   ORDO; Orphanet_98896; Duchenne muscular dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   1Y8M
CA   Telomerase immortalized cell line
DT   Created: 23-02-16; Last updated: 10-04-25; Version: 13
//
RX   PubMed=22040608; DOI=10.1186/2044-5040-1-34; PMCID=PMC3235972;
RA   Mamchaoui K., Trollet C., Bigot A., Negroni E., Chaouch S., Wolff A.,
RA   Kandalla P.K., Marie S., Di Santo J.P., St Guily J.L., Muntoni F.,
RA   Kim J., Philippi S., Spuler S., Levy N., Blumen S.C., Voit T.,
RA   Wright W.E., Aamiri A., Butler-Browne G.S., Mouly V.;
RT   "Immortalized pathological human myoblasts: towards a universal tool
RT   for the study of neuromuscular disorders.";
RL   Skelet. Muscle 1:34.1-34.11(2011).
//