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Peer Review reports

From: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report

Original Submission
12 Mar 2016 Submitted Original manuscript
10 Jul 2016 Reviewed Reviewer Report - Kamel Jabbari
16 Jan 2017 Reviewed Reviewer Report - Catherine SARRET
22 Mar 2017 Author responded Author comments - Jaber LYAHYAI
Resubmission - Version 2
22 Mar 2017 Submitted Manuscript version 2
28 Mar 2017 Reviewed Reviewer Report - Kamel Jabbari
6 Apr 2017 Reviewed Reviewer Report - Catherine SARRET
21 May 2017 Author responded Author comments - Jaber LYAHYAI
Resubmission - Version 3
21 May 2017 Submitted Manuscript version 3
10 Jul 2017 Author responded Author comments - Jaber LYAHYAI
Resubmission - Version 4
10 Jul 2017 Submitted Manuscript version 4
14 Feb 2018 Author responded Author comments - Jaber LYAHYAI
Resubmission - Version 5
14 Feb 2018 Submitted Manuscript version 5
Publishing
15 Feb 2018 Editorially accepted
27 Feb 2018 Article published 10.1186/s12887-018-1063-5

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