ID   GM27261
AC   CVCL_A2QD
DR   Coriell; GM27261
DR   Wikidata; Q105507108
CC   Population: Caucasian.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C176903; Rett syndrome, congenital variant
DI   ORDO; Orphanet_3095; Atypical Rett syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_A2QC ! GM27260
SX   Male
AG   2Y
CA   Finite cell line
DT   Created: 12-01-21; Last updated: 29-06-23; Version: 5
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