ID   GM10389
AC   CVCL_RB00
DR   CLO; CLO_0028569
DR   BioSample; SAMN00799981
DR   Coriell; GM10389
DR   Wikidata; Q54844429
RX   CelloPub=CLPUB00447;
CC   Population: African American.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C126741; Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 4
DI   ORDO; Orphanet_272; Congenital muscular dystrophy, Fukuyama type
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   7Y
CA   Finite cell line
DT   Created: 05-03-18; Last updated: 29-06-23; Version: 7
//
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).
//