ID   GM08024
AC   CVCL_IK46
DR   CLO; CLO_0010030
DR   Coriell; GM08024
DR   Wikidata; Q54843051
RX   CelloPub=CLPUB00447;
CC   Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
DI   NCIt; C103144; Perlman syndrome
DI   ORDO; Orphanet_2849; Perlman syndrom
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   30FW
CA   Finite cell line
DT   Created: 01-12-16; Last updated: 29-06-23; Version: 7
//
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 misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//