ID   WS7KO
AC   CVCL_A7PQ
SY   Werner Syndrome 7 KObe
DR   Wikidata; Q107117536
RX   PubMed=4083160;
CC   Population: Japanese.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3447; Werner syndrome
DI   ORDO; Orphanet_902; Werner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   47Y
CA   Finite cell line
DT   Created: 20-05-21; Last updated: 29-06-23; Version: 5
//
RX   PubMed=4083160; DOI=10.1007/978-1-4684-7853-2_23;
RA   Fujiwara, Yoshisada
RA   Kano, Yoshio
RA   Ichihashi, Masamitsu
RA   Nakao, Yoshinobu
RA   Matsumura, Toshiharu
RT   "Abnormal fibroblast aging and DNA replication in the Werner
RT   syndrome.";
RL   Adv. Exp. Med. Biol. 190:459-477(1985).
//