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Peer Review reports

From: Whole-exome sequencing identifies a novel missense variant within LOXHD1 causing rare hearing loss in a Chinese family

Original Submission
21 Nov 2018 Submitted Original manuscript
22 Dec 2018 Reviewed Reviewer Report - Jianjun Xiong
28 Dec 2018 Reviewed Reviewer Report - Yuan Li
8 Jan 2019 Author responded Author comments - Na Shen
Resubmission - Version 2
8 Jan 2019 Submitted Manuscript version 2
10 Jan 2019 Author responded Author comments - Na Shen
Resubmission - Version 3
10 Jan 2019 Submitted Manuscript version 3
Publishing
22 Jan 2019 Editorially accepted
13 Feb 2019 Article published 10.1186/s12881-019-0758-2

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