Peer Review reports
From: Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment
| Original Submission | ||
|---|---|---|
| 1 Mar 2018 | Submitted | Original manuscript |
| 1 Apr 2018 | Reviewed | Reviewer Report - Alejandro Schaffer |
| 9 Apr 2018 | Reviewed | Reviewer Report - Vassos Neocleous |
| 16 Apr 2018 | Reviewed | Reviewer Report - Constantinos Deltas |
| 8 May 2018 | Author responded | Author comments - Isabelle Schrauwen |
| Resubmission - Version 2 | ||
| 8 May 2018 | Submitted | Manuscript version 2 |
| 10 May 2018 | Reviewed | Reviewer Report - Vassos Neocleous |
| 11 May 2018 | Reviewed | Reviewer Report - Constantinos Deltas |
| 11 May 2018 | Reviewed | Reviewer Report - Alejandro Schaffer |
| 21 May 2018 | Author responded | Author comments - Isabelle Schrauwen |
| Resubmission - Version 3 | ||
| 21 May 2018 | Submitted | Manuscript version 3 |
| 23 May 2018 | Author responded | Author comments - Isabelle Schrauwen |
| Resubmission - Version 4 | ||
| 23 May 2018 | Submitted | Manuscript version 4 |
| Publishing | ||
| 24 May 2018 | Editorially accepted | |
| 20 Jul 2018 | Article published | 10.1186/s12881-018-0618-5 |
You can find further information about peer review here.