ID   77RD224
AC   CVCL_B5MG
DR   Wikidata; Q111732801
RX   PubMed=3337113;
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex unspecified
AG   Age unspecified
CA   Finite cell line
DT   Created: 17-03-22; Last updated: 29-06-23; Version: 4
//
RX   PubMed=3337113; PMCID=PMC1715319;
RA   Jaspers, Nicolaas G.J.
RA   Taalman, Rob Desire F.M.
RA   Baan, Carla C.
RT   "Patients with an inherited syndrome characterized by
RT   immunodeficiency, microcephaly, and chromosomal instability: genetic
RT   relationship to ataxia telangiectasia.";
RL   Am. J. Hum. Genet. 42:66-73(1988).
//