ID   GM16632
AC   CVCL_AK41
SY   PD720.F RV:FANCA; 720-Retro
DR   CLO; CLO_0017356
DR   Coriell; GM16632
DR   Wikidata; Q54848675
RX   PubMed=12361951;
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:3582; FANCA.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C125702; Fanconi anemia, complementation group A
DI   ORDO; Orphanet_84; Fanconi anemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_AK40 ! GM16631
SX   Female
AG   13Y
CA   Finite cell line
DT   Created: 02-05-16; Last updated: 19-12-24; Version: 9
//
RX   PubMed=12361951; DOI=10.1074/jbc.M207937200;
RA   Donahue, Sarah L.
RA   Campbell, Colin
RT   "A DNA double strand break repair defect in Fanconi anemia
RT   fibroblasts.";
RL   J. Biol. Chem. 277:46243-46247(2002).
//