ID   CCMi005-A
AC   CVCL_B3NP
SY   DMD4 C3
DR   hPSCreg; CCMi005-A
DR   Wikidata; Q110432689
RX   PubMed=35961103;
CC   From: Centro Cardiologico Monzino; Milan; Italy.
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; 2928; DMD; Unexplicit; Ex45-50del; Zygosity=Hemizygous (PubMed=35961103).
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
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)
SX   Male
AG   10Y
CA   Induced pluripotent stem cell
DT   Created: 16-12-21; Last updated: 29-06-23; Version: 6
//
RX   PubMed=35961103; DOI=10.1016/j.scr.2022.102889;
RA   Rovina D., Castiglioni E., Mallia S., Rabino M., Farini A.,
RA   Belicchi M., Di Giuseppe G., Gervasini C., Torrente Y., Pompilio G.,
RA   Gowran A.;
RT   "Reprogramming of dermal fibroblasts from a Duchenne muscular
RT   dystrophy patient carrying a deletion of exons 45-50 into an induced
RT   pluripotent stem cell line (CCMi005-A).";
RL   Stem Cell Res. 64:102889-102889(2022).
//