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Peer Review reports

From: Mutations in both SAMD9 and SLC19A2 genes caused complex phenotypes characterized by recurrent infection, dysphagia and profound deafness – a case report for dual diagnosis

Original Submission
11 Dec 2018 Submitted Original manuscript
12 Mar 2019 Reviewed Reviewer Report - Shouichi Ohga
10 Apr 2019 Reviewed Reviewer Report - Reviewer 2
28 May 2019 Author responded Author comments - Yan Zhang
Resubmission - Version 2
28 May 2019 Submitted Manuscript version 2
20 Jun 2019 Author responded Author comments - Yan Zhang
Resubmission - Version 3
20 Jun 2019 Submitted Manuscript version 3
9 Jul 2019 Reviewed Reviewer Report - Reviewer 2
23 Aug 2019 Author responded Author comments - Yan Zhang
Resubmission - Version 4
23 Aug 2019 Submitted Manuscript version 4
1 Sep 2019 Author responded Author comments - Yan Zhang
Resubmission - Version 5
1 Sep 2019 Submitted Manuscript version 5
7 Sep 2019 Author responded Author comments - Yan Zhang
Resubmission - Version 6
7 Sep 2019 Submitted Manuscript version 6
16 Sep 2019 Author responded Author comments - Yan Zhang
Resubmission - Version 7
16 Sep 2019 Submitted Manuscript version 7
Publishing
20 Sep 2019 Editorially accepted
21 Oct 2019 Article published 10.1186/s12887-019-1733-y

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