An endothelial growth factor receptor compound mutation of T790M substitution with exon 19 deletion in a previously untreated patient: a case report
Pre-publication versions of this article are available by contacting firstname.lastname@example.org.
|3 Aug 2018||Submitted||Original manuscript|
|24 Sep 2018||Reviewed||Reviewer Report - Gian Paolo Spinelli|
|6 Oct 2018||Reviewed||Reviewer Report - El Bairi Khalid|
|4 Nov 2018||Reviewed||Reviewer Report - Ahmet Emre Eskazan|
|17 Dec 2018||Author responded||Author comments - Juan Falla-Martinez|
|Resubmission - Version 2|
|17 Dec 2018||Submitted||Manuscript version 2|
|2 Jan 2019||Reviewed||Reviewer Report - Ahmet Emre Eskazan|
|5 Jan 2019||Reviewed||Reviewer Report - El Bairi Khalid|
|9 Jan 2019||Reviewed||Reviewer Report - Gian Paolo Spinelli|
|9 Feb 2019||Author responded||Author comments - Juan Falla-Martinez|
|Resubmission - Version 3|
|9 Feb 2019||Submitted||Manuscript version 3|
|8 Apr 2019||Editorially accepted|
|15 May 2019||Article published||10.1186/s13256-019-2075-y|
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