Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes
Pre-publication versions of this article are available by contacting email@example.com.
|31 Jan 2018||Submitted||Original manuscript|
|3 May 2018||Reviewed||Reviewer Report - Ambroise Wonkam|
|17 May 2018||Reviewed||Reviewer Report - Giulia Soldà|
|11 Jul 2018||Author responded||Author comments - Morag Lewis|
|Resubmission - Version 2|
|11 Jul 2018||Submitted||Manuscript version 2|
|26 Jul 2018||Reviewed||Reviewer Report - Ambroise Wonkam|
|6 Aug 2018||Reviewed||Reviewer Report - Giulia Soldà|
|15 Aug 2018||Author responded||Author comments - Morag Lewis|
|Resubmission - Version 3|
|15 Aug 2018||Submitted||Manuscript version 3|
|21 Aug 2018||Editorially accepted|
|4 Sep 2018||Article published||10.1186/s12920-018-0395-1|
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