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Peer Review reports

From: Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families

Original Submission
8 Jan 2013 Submitted Original manuscript
12 Mar 2013 Reviewed Reviewer Report - Mustafa Tekin
29 Mar 2013 Reviewed Reviewer Report - Tom Walsh
16 May 2013 Author responded Author comments - Soo Kyung Koo
Resubmission - Version 2
16 May 2013 Submitted Manuscript version 2
12 Jun 2013 Reviewed Reviewer Report - Tom Walsh
28 Jun 2013 Reviewed Reviewer Report - Mustafa Tekin
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
9 Jul 2013 Editorially accepted
17 Jul 2013 Article published 10.1186/1471-2350-14-72

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BMC Medical Genetics

ISSN: 1471-2350

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