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Peer Review reports

From: Novel compound heterozygous mutations in CNGA1in a Chinese family affected with autosomal recessive retinitis pigmentosa by targeted sequencing

Original Submission
10 Nov 2015 Submitted Original manuscript
22 Jan 2016 Reviewed Reviewer Report - Li Jia Chen
26 Jan 2016 Reviewed Reviewer Report - Jian Huan Chen
24 Feb 2016 Author responded Author comments - Min Wang
Resubmission - Version 2
24 Feb 2016 Submitted Manuscript version 2
29 Mar 2016 Author responded Author comments - Min Wang
Resubmission - Version 3
29 Mar 2016 Submitted Manuscript version 3
29 May 2016 Author responded Author comments - Min Wang
Resubmission - Version 4
29 May 2016 Submitted Manuscript version 4
Publishing
16 Jun 2016 Editorially accepted
8 Jul 2016 Article published 10.1186/s12886-016-0281-6

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BMC Ophthalmology

ISSN: 1471-2415

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