ID   AG01756
AC   CVCL_JE20
SY   AG-1756; AG 1756; AG1756
DR   Coriell; AG01756
DR   Wikidata; Q54609526
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=7253718;
CC   Discontinued: Coriell; AG01756; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C84940; Oculocerebrorenal syndrome
DI   ORDO; Orphanet_534; Oculocerebrorenal syndrome of Lowe
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   2Y6M
CA   Finite cell line
DT   Created: 15-05-17; Last updated: 29-06-23; Version: 9
//
RX   PubMed=7253718; DOI=10.1016/0047-6374(81)90027-0;
RA   Das, Nirmal K.
RA   Murphy, Donald G.
RT   "The National Institute on Aging repository cell cultures.";
RL   Mech. Ageing Dev. 16:1-17(1981).
//
RX   DOI=10.5962/bhl.title.4090;
RA   Coriell, Lewis Lemon
RA   Greene, Arthur E.
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 4th edition. October 1977.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977).
//