ID   GM03102
AC   CVCL_H189
DR   CLO; CLO_0013479
DR   BioSample; SAMN00808250
DR   Coriell; GM03102
DR   Wikidata; Q54837874
RX   CelloPub=CLPUB00447;
RX   PubMed=33333453;
CC   Population: Caucasian.
CC   Karyotypic information: 47,XXY (Coriell=GM03102).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C34752; Klinefelter syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_H188 ! GM03091
SX   Male
AG   18FW
CA   Finite cell line
DT   Created: 11-02-13; Last updated: 29-06-23; Version: 12
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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) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//
RX   PubMed=33333453; DOI=10.1016/j.scr.2020.102119;
RA   Fiacco E., Alowaysi M., Astro V., Adamo A.;
RT   "Generation of an iPSC cohort of isogenic iPSC lines (46-XY and
RT   47-XXY) from a non-mosaic Klinefelter syndrome patient (47-XXY)
RT   (KAUSTi008-A, KAUSTi008-B, KAUSTi008-C, KAUSTi008-D, KAUSTi008-E,
RT   KAUSTi008-F, KAUSTi008-G).";
RL   Stem Cell Res. 50:102119-102119(2021).
//