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Peer Review reports

From: Novel compound heterozygous mutations in OCA2 gene associated with non-syndromic oculocutaneous albinism in a Chinese Han patient: a case report

Original Submission
5 Feb 2019 Submitted Original manuscript
15 Mar 2019 Reviewed Reviewer Report - Benoît Arveiler
9 May 2019 Reviewed Reviewer Report - Kunal Ray
25 May 2019 Author responded Author comments - Hairong Wang
Resubmission - Version 2
25 May 2019 Submitted Manuscript version 2
13 Jun 2019 Author responded Author comments - Hairong Wang
Resubmission - Version 3
13 Jun 2019 Submitted Manuscript version 3
Publishing
19 Jun 2019 Editorially accepted
25 Jul 2019 Article published 10.1186/s12881-019-0850-7

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