ID   AG09233
AC   CVCL_0N76
DR   CLO; CLO_0021733
DR   Coriell; AG09233
DR   Wikidata; Q54742832
RX   CelloPub=CLPUB00597;
RX   PubMed=12768443;
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C121565; Neonatal progeroid syndrome
DI   ORDO; Orphanet_3455; Wiedemann-Rautenstrauch syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_0N77 ! AG09279
SX   Male
AG   8M
CA   Finite cell line
DT   Created: 10-04-15; Last updated: 29-06-23; Version: 10
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RX   CelloPub=CLPUB00597;
RG   National Institute on Aging;
RT   "1994 catalog of cell lines. NIA Aging Cell Repository.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-351; National Institutes of Health; Bethesda; USA (1994).
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RX   PubMed=12768443; DOI=10.1007/s10038-003-0025-3;
RA   Cao H.-N., Hegele R.A.;
RT   "LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not
RT   in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090).";
RL   J. Hum. Genet. 48:271-274(2003).
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