ID   GM00172
AC   CVCL_CV48
SY   GM 172
DR   Coriell; GM00172
DR   Wikidata; Q54836075
CC   Discontinued: Coriell; GM00172; probable.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C3447; Werner syndrome
DI   ORDO; Orphanet_902; Werner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
CA   Finite cell line
DT   Created: 13-07-16; Last updated: 29-06-23; Version: 6
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