ID   CS3IAF
AC   CVCL_ZT17
DR   Wikidata; Q98125754
RX   PubMed=8834235;
CC   Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
DI   NCIt; C135725; Cockayne syndrome type A
DI   ORDO; Orphanet_191; Cockayne syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex unspecified
AG   Fetus
CA   Finite cell line
DT   Created: 02-07-20; Last updated: 29-06-23; Version: 4
//
RX   PubMed=8834235; DOI=10.1007/BF02267059;
RA   Stefanini, Miria
RA   Fawcett, Heather
RA   Botta, Elena
RA   Nardo, Tiziana
RA   Lehmann, Alan Robert
RT   "Genetic analysis of twenty-two patients with Cockayne syndrome.";
RL   Hum. Genet. 97:418-423(1996).
//