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Peer Review reports

From: A novel delins (c.773_819+47delinsAA) mutation of the PCCA gene associated with neonatal-onset propionic acidemia: a case report

Original Submission
19 Mar 2019 Submitted Original manuscript
4 Jul 2019 Reviewed Reviewer Report
16 Jul 2019 Reviewed Reviewer Report - Neerja Gupta
4 Feb 2020 Reviewed Reviewer Report
5 May 2020 Author responded Author comments - Hai-rong Wang
Resubmission - Version 2
5 May 2020 Submitted Manuscript version 2
19 May 2020 Reviewed Reviewer Report
23 May 2020 Reviewed Reviewer Report
1 Jun 2020 Author responded Author comments - Hai-rong Wang
Resubmission - Version 3
1 Jun 2020 Submitted Manuscript version 3
9 Jun 2020 Author responded Author comments - Hai-rong Wang
Resubmission - Version 4
9 Jun 2020 Submitted Manuscript version 4
Publishing
5 Aug 2020 Editorially accepted
20 Aug 2020 Article published 10.1186/s12881-020-01102-1

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