ID   GM10259
AC   CVCL_AD99
DR   CLO; CLO_0029209
DR   BioSample; SAMN00799855
DR   Coriell; GM10259
DR   Wikidata; Q54844328
RX   CelloPub=CLPUB00447;
RX   PubMed=2748491;
CC   Population: Hispanic.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C84794; Jeune syndrome
DI   ORDO; Orphanet_474; Jeune syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   7D
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 29-06-23; Version: 8
//
RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//
RX   PubMed=2748491; DOI=10.3109/15513818909037734;
RA   Knisely A.S., Steigman C.K.;
RT   "Stenosis of the foramen magnum and rostral spinal canal, with spinal
RT   cord deformity, in Jeune's asphyxiating thoracic dystrophy.";
RL   Pediatr. Pathol. 9:299-305(1989).
//