Open AccessSomatic loss of function mutations in neurofibromin 1 and MYC associated factor X genes identified by exome-wide sequencing in a wild-type GIST case
Author(s) -
Martin G. Belinsky,
Lori Rink,
Kathy Q. Cai,
Stephen J. Capuzzi,
Hoang Yen,
Jeremy Chien,
Andrew K. Godwin,
Margaret Mehren
Publication year - 2015
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/y3pb-1k59
Subject(s) - neurofibromin 1 , exome sequencing , somatic cell , biology , gist , genetics , gene , exome , mutation , wild type , loss function , germline mutation , cancer research , mutant , phenotype , stromal cell