ID   NH50139
AC   CVCL_UY56
DR   NHCDR; NH50139
DR   Wikidata; Q98127563
CC   Population: Caucasian.
CC   Donor information: At sampling donor was not affected with autosomal dominant torsion dystonia 1 but at risk for disease.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C118780; Autosomal dominant torsion dystonia 1
DI   ORDO; Orphanet_256; Early-onset generalized limb-onset dystonia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   57Y
CA   Finite cell line
DT   Created: 25-02-19; Last updated: 29-06-23; Version: 7
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