Skip to main content

Peer Review reports

From: Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with bone disease severity in Rett syndrome

Original Submission
16 Jun 2019 Submitted Original manuscript
20 Jul 2019 Author responded Author comments - Carla Caffarelli
Resubmission - Version 2
20 Jul 2019 Submitted Manuscript version 2
25 Aug 2019 Reviewed Reviewer Report - Jawasd Fares
10 Dec 2019 Reviewed Reviewer Report - Milica Keckarevic Markovic
5 Jan 2020 Author responded Author comments - Carla Caffarelli
Resubmission - Version 3
5 Jan 2020 Submitted Manuscript version 3
21 Jan 2020 Author responded Author comments - Carla Caffarelli
Resubmission - Version 4
21 Jan 2020 Submitted Manuscript version 4
Publishing
23 Jan 2020 Editorially accepted
31 Jan 2020 Article published 10.1186/s12881-020-0960-2

You can find further information about peer review here.

Back to article page