ID   GM24256
AC   CVCL_AZ18
DR   Coriell; GM24256
DR   Wikidata; Q54853669
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C118783; Merosin-deficient congenital muscular dystrophy type 1A
DI   ORDO; Orphanet_258; Laminin subunit alpha 2-related congenital muscular dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_AZ15 ! GM24253
SX   Male
AG   7Y
CA   Finite cell line
DT   Created: 02-05-16; Last updated: 29-06-23; Version: 7
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