ID   XP165MA
AC   CVCL_4T40
DR   Wikidata; Q54994889
RX   PubMed=23370536;
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3969; Xeroderma pigmentosum, complementation group G
DI   ORDO; Orphanet_910; Xeroderma pigmentosum
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 29-06-23; Version: 6
//
RX   PubMed=23370536; DOI=10.1038/jid.2013.54;
RA   Schafer, Annika
RA   Schubert, Steffen
RA   Gratchev, Alexei
RA   Seebode, Christina
RA   Apel, Antje
RA   Laspe, Petra
RA   Hofmann, Lars
RA   Ohlenbusch, Andreas
RA   Mori, Toshio
RA   Kobayashi, Nobuhiko
RA   Schurer, Anke
RA   Schon, Michael P.
RA   Emmert, Steffen
RT   "Characterization of three XPG-defective patients identifies three
RT   missense mutations that impair repair and transcription.";
RL   J. Invest. Dermatol. 133:1841-1849(2013).
//