Somatic loss of function mutations in neurofibromin 1 and MYC associated factor X genes identified by exome-wide sequencing in a wild-type GIST case
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|22 Jul 2015||Submitted||Original manuscript|
|28 Aug 2015||Reviewed||Reviewer Report - Shiva Keshava|
|28 Aug 2015||Reviewed||Reviewer Report - Ghanshyam Upadhyay|
|9 Sep 2015||Author responded||Author comments - Martin Belinsky|
|Resubmission - Version 2|
|9 Sep 2015||Submitted||Manuscript version 2|
|16 Oct 2015||Author responded||Author comments - Martin Belinsky|
|Resubmission - Version 3|
|16 Oct 2015||Submitted||Manuscript version 3|
|30 Oct 2015||Editorially accepted|
|10 Nov 2015||Article published||10.1186/s12885-015-1872-y|
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