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Peer Review reports

From: Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family

Original Submission
20 Sep 2017 Submitted Original manuscript
27 Sep 2017 Author responded Author comments - Liena Elsayed
Resubmission - Version 2
27 Sep 2017 Submitted Manuscript version 2
3 Oct 2017 Author responded Author comments - Liena Elsayed
Resubmission - Version 3
3 Oct 2017 Submitted Manuscript version 3
14 Nov 2017 Reviewed Reviewer Report - Aravindhan Veerapandiyan
27 Dec 2017 Reviewed Reviewer Report - Parayil Sankaran Bindu
2 Jan 2018 Reviewed Reviewer Report - Carlotta Spagnoli
2 Feb 2018 Author responded Author comments - Liena Elsayed
Resubmission - Version 4
2 Feb 2018 Submitted Manuscript version 4
8 Feb 2018 Reviewed Reviewer Report - Aravindhan Veerapandiyan
20 Feb 2018 Reviewed Reviewer Report - Parayil Sankaran Bindu
16 Mar 2018 Author responded Author comments - Liena Elsayed
Resubmission - Version 5
16 Mar 2018 Submitted Manuscript version 5
17 Mar 2018 Reviewed Reviewer Report - Aravindhan Veerapandiyan
19 Apr 2018 Author responded Author comments - Liena Elsayed
Resubmission - Version 6
19 Apr 2018 Submitted Manuscript version 6
Publishing
24 Apr 2018 Editorially accepted
8 May 2018 Article published 10.1186/s12881-018-0592-y

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