ID   INSRMi009-A
AC   CVCL_A2XW
SY   DMD_RaPer_PhyMedExp
DR   hPSCreg; INSRMi009-A
DR   Wikidata; Q105509671
RX   PubMed=33246213;
CC   From: INSERM; Paris; France.
CC   Sequence variation: Mutation; HGNC; HGNC:2928; DMD; Unexplicit; Ex52del; Zygosity=Hemizygous (PubMed=33246213).
CC   Omics: Variations; Array-based CGH.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C75482; Duchenne muscular dystrophy
DI   ORDO; Orphanet_98896; Duchenne muscular dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   12Y
CA   Induced pluripotent stem cell
DT   Created: 12-01-21; Last updated: 10-04-25; Version: 6
//
RX   PubMed=33246213; DOI=10.1016/j.scr.2020.102094;
RA   Souidi, Monia
RA   Amedro, Pascal
RA   Meyer, Pierre
RA   Desprat, Romain
RA   Lemaitre, Jean-Marc
RA   Rivier, Francois
RA   Lacampagne, Alain
RA   Meli, Albano Carlo
RT   "Generation of three Duchenne muscular dystrophy patient-specific
RT   induced pluripotent stem cell lines DMD_YoTaz_PhyMedEXp,
RT   DMD_RaPer_PhyMedEXp, DMD_OuMen_PhyMedEXp (INSRMi008-A, INSRMi009-A and
RT   INSRMi010-A).";
RL   Stem Cell Res. 49:102094-102094(2020).
//