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Peer Review reports

From: A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability

Original Submission
25 Feb 2022 Submitted Original manuscript
3 Mar 2022 Author responded Author comments - Mutaz Amin
Resubmission - Version 2
3 Mar 2022 Submitted Manuscript version 2
26 Mar 2022 Reviewed Reviewer Report
26 Apr 2022 Reviewed Reviewer Report
28 Apr 2022 Author responded Author comments - Mutaz Amin
Resubmission - Version 3
28 Apr 2022 Submitted Manuscript version 3
19 May 2022 Author responded Author comments - Mutaz Amin
Resubmission - Version 4
19 May 2022 Submitted Manuscript version 4
26 May 2022 Author responded Author comments - Mutaz Amin
Resubmission - Version 5
26 May 2022 Submitted Manuscript version 5
31 Aug 2022 Author responded Author comments - Mutaz Amin
Resubmission - Version 6
31 Aug 2022 Submitted Manuscript version 6
5 Sep 2022 Author responded Author comments - Mutaz Amin
Resubmission - Version 7
5 Sep 2022 Submitted Manuscript version 7
Publishing
9 Sep 2022 Editorially accepted
8 Nov 2022 Article published 10.1186/s12920-022-01354-1

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