ID   DMD-iPS (DYS-HAC)4
AC   CVCL_C984
DR   SKIP; SKIP001468
DR   Wikidata; Q54831279
RX   PubMed=19997091;
CC   From: Tottori University; Tottori; Japan.
CC   Sequence variation: Mutation; HGNC; HGNC:2928; DMD; Unexplicit; Ex4-43del; Zygosity=Hemizygous (from parent cell line).
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)
HI   CVCL_L752 ! GM05169
SX   Male
AG   9Y
CA   Induced pluripotent stem cell
DT   Created: 22-10-12; Last updated: 19-12-24; Version: 16
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RX   PubMed=19997091; DOI=10.1038/mt.2009.274; PMCID=PMC2839293;
RA   Kazuki Y., Hiratsuka M., Takiguchi M., Osaki M., Kajitani N.,
RA   Hoshiya H., Hiramatsu K., Yoshino T., Kazuki K., Ishihara C.,
RA   Takehara S., Higaki K., Nakagawa M., Takahashi K., Yamanaka S.,
RA   Oshimura M.;
RT   "Complete genetic correction of iPS cells from Duchenne muscular
RT   dystrophy.";
RL   Mol. Ther. 18:386-393(2010).
//