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Peer Review reports

From: PHKA2 mutation spectrum in Korean patients with glycogen storage disease type IX: prevalence of deletion mutations

Original Submission
29 Aug 2015 Submitted Original manuscript
23 Oct 2015 Reviewed Reviewer Report - Deeksha S. Bali
25 Oct 2015 Reviewed Reviewer Report - Nelson L.S. Tang
27 Nov 2015 Author responded Author comments - Rihwa Choi
Resubmission - Version 2
27 Nov 2015 Submitted Manuscript version 2
Publishing
14 Apr 2016 Editorially accepted
21 Apr 2016 Article published 10.1186/s12881-016-0295-1

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