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Peer Review reports

From: A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family

Original Submission
8 Feb 2020 Submitted Original manuscript
13 Feb 2020 Author responded Author comments - Akram Sarmadi
23 Mar 2020 Reviewed Reviewer Report - Nadia Al-Wardy
29 Mar 2020 Reviewed Reviewer Report - Semra Gürsoy
13 Apr 2020 Reviewed Reviewer Report - Abdullah Gibriel
10 May 2020 Author responded Author comments - Akram Sarmadi
Resubmission - Version 2
13 Feb 2020 Submitted Manuscript version 2
12 May 2020 Reviewed Reviewer Report - Abdullah Gibriel
13 May 2020 Reviewed Reviewer Report - Semra Gürsoy
21 May 2020 Author responded Author comments - Akram Sarmadi
Resubmission - Version 3
21 May 2020 Submitted Manuscript version 3
30 May 2020 Author responded Author comments - Akram Sarmadi
Resubmission - Version 4
30 May 2020 Submitted Manuscript version 4
Publishing
2 Jun 2020 Editorially accepted
9 Jun 2020 Article published 10.1186/s12881-020-01061-7

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