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Peer Review reports

From: A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: clinical course and response to riboflavin

Original Submission
14 Jan 2019 Submitted Original manuscript
26 Feb 2019 Reviewed Reviewer Report - Manoj Menezes
1 Mar 2019 Reviewed Reviewer Report - BALASUBRAMANIEM ASHOK KUMAR
5 Mar 2019 Reviewed Reviewer Report - Maria Barile
4 Apr 2019 Author responded Author comments - Kaili Shi
Resubmission - Version 2
4 Apr 2019 Submitted Manuscript version 2
17 Apr 2019 Author responded Author comments - Kaili Shi
Resubmission - Version 3
17 Apr 2019 Submitted Manuscript version 3
Publishing
23 Apr 2019 Editorially accepted
7 May 2019 Article published 10.1186/s12881-019-0811-1

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