ID   AG03848
SY   AG 3848; AG3848; SMA2FABE
DR   Coriell; AG03848
DR   Wikidata; Q105506266
RX   CelloPub=CLPUB00387;
RX   PubMed=3941662;
RX   PubMed=7253718;
CC   Discontinued: Coriell; AG03848; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C98670; Werdnig-Hoffmann disease
DI   ORDO; Orphanet_83330; Proximal spinal muscular atrophy type 1
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   6Y
CA   Finite cell line
DT   Created: 12-01-21; Last updated: 29-06-23; Version: 5
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   PubMed=3941662; DOI=10.1016/0027-5107(86)90121-1;
RA   Scudiero D.A., Polinsky R.J., Brumback R.A., Tarone R.E., Nee L.E.,
RA   Robbins J.H.;
RT   "Alzheimer disease fibroblasts are hypersensitive to the lethal effects
RT   of a DNA-damaging chemical.";
RL   Mutat. Res. 159:125-131(1986).
RX   PubMed=7253718; DOI=10.1016/0047-6374(81)90027-0;
RA   Das N.K., Murphy D.G.;
RT   "The National Institute on Aging repository cell cultures.";
RL   Mech. Ageing Dev. 16:1-17(1981).