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Peer Review reports

From: Homozygous variants in the HEXB and MBOAT7 genes underlie neurological diseases in consanguineous families

Original Submission
22 May 2019 Submitted Original manuscript
18 Jul 2019 Reviewed Reviewer Report - Ahmed Bouhouche
25 Jul 2019 Reviewed Reviewer Report - Esra Dikoglu
26 Jul 2019 Reviewed Reviewer Report - Juan Rodriguez-Flores
7 Sep 2019 Author responded Author comments - Asma Gul
Resubmission - Version 2
7 Sep 2019 Submitted Manuscript version 2
5 Oct 2019 Author responded Author comments - Shazia Khan
Resubmission - Version 3
5 Oct 2019 Submitted Manuscript version 3
8 Oct 2019 Author responded Author comments - Shazia Khan
Resubmission - Version 4
8 Oct 2019 Submitted Manuscript version 4
9 Oct 2019 Author responded Author comments - Shazia Khan
Resubmission - Version 5
9 Oct 2019 Submitted Manuscript version 5
Publishing
15 Oct 2019 Editorially accepted
18 Dec 2019 Article published 10.1186/s12881-019-0907-7

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