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Peer Review reports

From: Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A

Original Submission
17 Jun 2022 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
16 Jul 2022 Reviewed Reviewer Report
29 Jul 2022 Reviewed Reviewer Report - Farshid Parvini
17 Aug 2022 Author responded Author comments - Xue Gao
Resubmission - Version 3
17 Aug 2022 Submitted Manuscript version 3
20 Aug 2022 Author responded Author comments - Xue Gao
Resubmission - Version 4
20 Aug 2022 Submitted Manuscript version 4
30 Aug 2022 Reviewed Reviewer Report
11 Sep 2022 Reviewed Reviewer Report - Farshid Parvini
22 Sep 2022 Author responded Author comments - Xue Gao
Resubmission - Version 5
22 Sep 2022 Submitted Manuscript version 5
Publishing
29 Sep 2022 Editorially accepted
18 Nov 2022 Article published 10.1186/s12920-022-01368-9

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BMC Medical Genomics

ISSN: 1755-8794

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