ID   GM24260
AC   CVCL_AZ20
DR   Coriell; GM24260
DR   Wikidata; Q54853673
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_AZ16 ! GM24254
SX   Female
AG   8Y
CA   Finite cell line
DT   Created: 02-05-16; Last updated: 29-06-23; Version: 7
//