ID   GM25313
AC   CVCL_5T43
SY   GM25313*D
DR   Coriell; GM25313
DR   SKIP; SKIP001196
DR   Wikidata; Q54853871
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:2928; DMD; Unexplicit; Ex45del; Zygosity=Hemizygous (Coriell=GM25313).
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_5N08 ! GM05112
SX   Male
AG   13Y
CA   Induced pluripotent stem cell
DT   Created: 23-02-16; Last updated: 19-12-24; Version: 12
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