ID   GM02663
AC   CVCL_AW99
SY   GM2663
DR   CLO; CLO_0014972
DR   Coriell; GM02663
DR   Wikidata; Q54837608
RX   CelloPub=CLPUB00387;
RX   CelloPub=CLPUB00447;
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C126559; Hard skin syndrome Parana type
DI   ORDO; Orphanet_2812; Parana hard skin syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   13Y
CA   Finite cell line
DT   Created: 02-05-16; Last updated: 29-06-23; Version: 9
//
RX   CelloPub=CLPUB00387;
RA   Coriell L.L., Greene A.E., Mulivor R.A.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 7th edition. October 1980.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 80-2011; pp.1-254; National Institutes of Health; Bethesda (1980).
//
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).
//