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Peer Review reports

From: Targeted exome sequencing reveals novel USH2A mutations in Chinese patients with simplex Usher syndrome

Original Submission
27 Dec 2014 Submitted Original manuscript
Author responded Author comments
Reviewed Reviewer Report
Reviewed Reviewer Report
Resubmission - Version 2
Submitted Manuscript version 2
Resubmission - Version 3
Submitted Manuscript version 3
Author responded Author comments
Resubmission - Version 4
Submitted Manuscript version 4
Author responded Author comments
Resubmission - Version 5
Submitted Manuscript version 5
Publishing
21 Aug 2015 Editorially accepted
16 Sep 2015 Article published 10.1186/s12881-015-0223-9

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