ID   GM23892
AC   CVCL_4T54
DR   Coriell; GM23892
DR   Wikidata; Q54853423
CC   Derived from site: In situ; Muscle; UBERON=UBERON_0001630.
CC   Cell type: Fibroblast of muscle; CL=CL_1001609.
DI   NCIt; C123438; Ullrich congenital muscular dystrophy
DI   ORDO; Orphanet_75840; Congenital muscular dystrophy, Ullrich type
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   3Y
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 29-06-23; Version: 8
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