ID   CSHM1FABE
AC   CVCL_C3Q8
SY   Cockayne Syndrome Heterozygous Male 1 FArgo BEthesda; GM05322; RB 5322
DR   Coriell; GM05322
DR   Wikidata; Q116048802
RX   PubMed=6096450;
CC   Discontinued: Coriell; GM05322; probable.
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)
OI   CVCL_C3Q9 ! CSHM1FABE LCL
SX   Male
AG   30Y
CA   Finite cell line
DT   Created: 15-12-22; Last updated: 29-06-23; Version: 3
//
RX   PubMed=6096450; DOI=10.1111/1523-1747.ep12260999;
RA   Otsuka, Fujio
RA   Tarone, Robert E.
RA   Cayeux, Sophie
RA   Robbins, Jay H.
RT   "Use of lymphoblastoid cell lines to evaluate the hypersensitivity to
RT   ultraviolet radiation in Cockayne syndrome.";
RL   J. Invest. Dermatol. 82:480-484(1984).
//