ID   CS267BE
AC   CVCL_EG47
SY   Cockayne Syndrome 267 BEthesda; GM11551
DR   CLO; CLO_0021057
DR   Coriell; GM11551
DR   Wikidata; Q54845152
RX   PubMed=12060391;
CC   Population: Caucasian.
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)
OI   CVCL_EG46 ! CS267BE LCL
SX   Female
AG   16Y
CA   Finite cell line
DT   Created: 13-07-16; Last updated: 29-06-23; Version: 8
//
RX   PubMed=12060391; DOI=10.1046/j.1523-1747.2002.01782.x;
RA   Emmert, Steffen
RA   Slor, Hanoch
RA   Busch, David B.
RA   Batko, Sima
RA   Albert, Roberta B.
RA   Coleman, Donna M.
RA   Khan, Sikandar G.
RA   Abu-Libdeh, Bassam
RA   DiGiovanna, John Joseph
RA   Cunningham, Bari Bickel
RA   Lee, Myung-Moo
RA   Crollick, Jill
RA   Inui, Hiroki
RA   Ueda, Takahiro
RA   Hedayati, Mohammad
RA   Grossman, Lawrence
RA   Shahlavi, Tala
RA   Cleaver, James Edward
RA   Kraemer, Kenneth H.
RT   "Relationship of neurologic degeneration to genotype in three
RT   xeroderma pigmentosum group G patients.";
RL   J. Invest. Dermatol. 118:972-982(2002).
//