ID   GM00361
AC   CVCL_V828
SY   GM-361; GM00966; GM-966
DR   Coriell; GM00361
DR   Coriell; GM00966
DR   Wikidata; Q54836179
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=177249;
CC   Discontinued: Coriell; GM00361; probable.
CC   Discontinued: Coriell; GM00966; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C123416; Hyperlipoproteinemia, type IIa
DI   ORDO; Orphanet_391665; Homozygous familial hypercholesterolemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   12Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 11
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RX   PubMed=177249; DOI=10.1159/000130531;
RA   Goldstein, Joseph Leonard
RA   Brown, Michael Stuart
RA   Greene, Arthur E.
RA   Coriell, Lewis Lemon
RT   "Homozygous familial hypercholesterolemia (receptor-negative type).
RT   Repository identification No. GM-361.";
RL   Cytogenet. Cell Genet. 15:357-359(1975).
//
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).
//