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Peer Review reports

From: Two novel compound heterozygous mutations in NGLY1as a cause of congenital disorder of deglycosylation: a case presentation

Original Submission
10 Mar 2020 Submitted Original manuscript
25 Mar 2020 Reviewed Reviewer Report - Hanneke Haijes
30 Apr 2020 Reviewed Reviewer Report
25 May 2020 Author responded Author comments - haixia ge
Resubmission - Version 2
25 May 2020 Submitted Manuscript version 2
4 Jun 2020 Author responded Author comments - haixia ge
Resubmission - Version 3
4 Jun 2020 Submitted Manuscript version 3
6 Jun 2020 Author responded Author comments - haixia ge
Resubmission - Version 4
6 Jun 2020 Submitted Manuscript version 4
Publishing
10 Jun 2020 Editorially accepted
23 Jun 2020 Article published 10.1186/s12881-020-01067-1

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