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Peer Review reports

From: A novel RAB39B mutation and concurrent de novo NF1 mutation in a boy with neurofibromatosis type 1, intellectual disability, and autism: a case report

Original Submission
3 Jul 2020 Submitted Original manuscript
7 Aug 2020 Reviewed Reviewer Report
9 Aug 2020 Reviewed Reviewer Report
14 Aug 2020 Author responded Author comments - Claudia Santoro
Resubmission - Version 2
14 Aug 2020 Submitted Manuscript version 2
24 Aug 2020 Author responded Author comments - Claudia Santoro
Resubmission - Version 3
24 Aug 2020 Submitted Manuscript version 3
Publishing
26 Aug 2020 Editorially accepted
1 Sep 2020 Article published 10.1186/s12883-020-01911-0

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