ID   CS2BR
AC   CVCL_ZN62
SY   Cockayne Syndrome 2 BRighton
DR   Wikidata; Q98125741
RX   PubMed=8834235;
RX   PubMed=18079351;
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C135726; Cockayne syndrome type B
DI   ORDO; Orphanet_191; Cockayne syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex unspecified
AG   10Y
CA   Finite cell line
DT   Created: 02-07-20; Last updated: 29-06-23; Version: 5
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RX   PubMed=8834235; DOI=10.1007/BF02267059;
RA   Stefanini, Miria
RA   Fawcett, Heather
RA   Botta, Elena
RA   Nardo, Tiziana
RA   Lehmann, Alan Robert
RT   "Genetic analysis of twenty-two patients with Cockayne syndrome.";
RL   Hum. Genet. 97:418-423(1996).
//
RX   PubMed=18079351; DOI=10.1259/bjr/27072321;
RA   Arlett, Colin Francis
RA   Green, Michael H.L.
RA   Rogers, Paul Bryan
RA   Lehmann, Alan Robert
RA   Plowman, Piers N.
RT   "Minimal ionizing radiation sensitivity in a large cohort of xeroderma
RT   pigmentosum fibroblasts.";
RL   Br. J. Radiol. 81:51-58(2008).
//