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Peer Review reports

From: Discovery of sensorineural hearing loss and ossicle deformity in a Chinese Li nationality family with spondyloepiphyseal dysplasia congenita caused by p.G504S mutation of COL2A1

Original Submission
16 Dec 2020 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
22 Dec 2020 Reviewed Reviewer Report
27 Dec 2020 Reviewed Reviewer Report
8 Apr 2021 Author responded Author comments - Qiujing Zhang
Resubmission - Version 3
8 Apr 2021 Submitted Manuscript version 3
Resubmission - Version 4
Submitted Manuscript version 4
12 May 2021 Reviewed Reviewer Report
21 May 2021 Reviewed Reviewer Report
Resubmission - Version 5
Submitted Manuscript version 5
Publishing
24 May 2021 Editorially accepted
28 Jun 2021 Article published 10.1186/s12920-021-01020-y

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