ID   Kps4
AC   CVCL_ZT09
DR   Wikidata; Q98126840
RX   PubMed=7513056;
CC   Population: Japanese.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3965; Xeroderma pigmentosum, complementation group A
DI   ORDO; Orphanet_910; Xeroderma pigmentosum
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
CA   Finite cell line
DT   Created: 02-07-20; Last updated: 29-06-23; Version: 5
//
RX   PubMed=7513056; DOI=10.1016/0921-8777(94)90068-x;
RA   Itoh, Toshiki
RA   Ono, Tomomichi
RA   Yamaizumi, Masaru
RT   "A new UV-sensitive syndrome not belonging to any complementation
RT   groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing
RT   biochemical characteristics of Cockayne syndrome without typical
RT   clinical manifestations.";
RL   Mutat. Res. 314:233-248(1994).
//