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Peer Review reports

From: Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)

Original Submission
28 Mar 2016 Submitted Original manuscript
24 Apr 2016 Reviewed Reviewer Report - Rui Chen
25 Sep 2016 Reviewed Reviewer Report - Sheikh Riazuddin
5 Mar 2017 Author responded Author comments - Shari Javadiyan
Resubmission - Version 2
5 Mar 2017 Submitted Manuscript version 2
14 Apr 2017 Reviewed Reviewer Report - Sheikh Riazuddin
18 Apr 2017 Author responded Author comments - Shari Javadiyan
Resubmission - Version 3
18 Apr 2017 Submitted Manuscript version 3
19 Apr 2017 Author responded Author comments - Shari Javadiyan
Resubmission - Version 4
19 Apr 2017 Submitted Manuscript version 4
Publishing
28 Apr 2017 Editorially accepted
8 May 2017 Article published 10.1186/s12881-017-0414-7

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