ID   CS1MO
AC   CVCL_ZP14
SY   Cockayne Syndrome 1 MOriguchi
DR   JCRB; KURB1885
DR   JCRB; KURB1886
DR   Wikidata; Q98125731
RX   PubMed=9777763;
CC   Population: Japanese.
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   Female
AG   Children
CA   Finite cell line
DT   Created: 02-07-20; Last updated: 29-06-23; Version: 5
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RX   PubMed=9777763; DOI=10.1016/S0190-9622(98)70005-2;
RA   Miyauchi-Hashimoto, Hiroko
RA   Akaeda, Tamiyo
RA   Maihara, Toshiro
RA   Ikenaga, Mituo
RA   Horio, Takeshi
RT   "Cockayne syndrome without typical clinical manifestations including
RT   neurologic abnormalities.";
RL   J. Am. Acad. Dermatol. 39:565-570(1998).
//