ID   TTD1GL
AC   CVCL_ZU59
SY   TrichoThioDystrophy 1 GLascow; P1
DR   Wikidata; Q98133657
RX   PubMed=2458832;
RX   PubMed=6492094;
CC   Population: Caucasian; Scottish.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C4924; Trichothiodystrophy
DI   ORDO; Orphanet_33364; Trichothiodystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   4Y
CA   Finite cell line
DT   Created: 02-07-20; Last updated: 29-06-23; Version: 5
//
RX   PubMed=2458832;
RA   Lehmann A.R., Arlett C.F., Broughton B.C., Harcourt S.A.,
RA   Steingrimsdottir H., Stefanini M., Taylor A.M.R., Natarajan A.T.,
RA   Green S., King M.D., MacKie R.M., Stephenson J.B.P., Tolmie J.L.;
RT   "Trichothiodystrophy, a human DNA repair disorder with heterogeneity
RT   in the cellular response to ultraviolet light.";
RL   Cancer Res. 48:6090-6096(1988).
//
RX   PubMed=6492094; DOI=10.1136/jmg.21.4.286; PMCID=PMC1049299;
RA   King M.D., Gummer C.L., Stephenson J.B.P.;
RT   "Trichothiodystrophy-neurotrichocutaneous syndrome of Pollitt: a
RT   report of two unrelated cases.";
RL   J. Med. Genet. 21:286-289(1984).
//