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Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report

Contributed equally
BMC Medical GeneticsBMC series – open, inclusive and trusted201718:151

https://doi.org/10.1186/s12881-017-0511-7

Received: 3 July 2017

Accepted: 8 December 2017

Published: 19 December 2017

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Open Peer Review reports

Pre-publication versions of this article are available by contacting info@biomedcentral.com.

Original Submission
3 Jul 2017 Submitted Original manuscript
8 Aug 2017 Reviewed Reviewer Report - Karen Friderici
3 Oct 2017 Reviewed Reviewer Report - Trevor Lucas
12 Nov 2017 Author responded Author comments - Hye Ji Choi
Resubmission - Version 2
12 Nov 2017 Submitted Manuscript version 2
28 Nov 2017 Reviewed Reviewer Report - Trevor Lucas
5 Dec 2017 Reviewed Reviewer Report - Karen Friderici
8 Dec 2017 Author responded Author comments - Hye Ji Choi
Resubmission - Version 3
8 Dec 2017 Submitted Manuscript version 3
Publishing
8 Dec 2017 Editorially accepted
19 Dec 2017 Article published 10.1186/s12881-017-0511-7

How does Open Peer Review work?

Open peer review is a system where authors know who the reviewers are, and the reviewers know who the authors are. If the manuscript is accepted, the named reviewer reports are published alongside the article. Pre-publication versions of the article are available by contacting info@biomedcentral.com.

You can find further information about the peer review system here.

Authors’ Affiliations

(1)
Department of Otorhinolaryngology, Brain Korea 21 PLUS Project for Medical Sciences, Yonsei University College of Medicine, Seoul, South Korea
(2)
Department of Pharmacology, Brain Korea 21 PLUS Project for Medical Sciences, Yonsei University College of Medicine, Seoul, South Korea
(3)
Department of Otorhinolaryngology, Soonchunhyang University College of Medicine, Bucheon, South Korea
(4)
Yonsei University College of Medicine, Seoul, South Korea

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