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Peer Review reports

From: Severe clinical manifestation of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency associated with two novel mutations: a case report

Original Submission
24 May 2019 Submitted Original manuscript
8 Jul 2019 Reviewed Reviewer Report - Keiichi Hirono
10 Jul 2019 Reviewed Reviewer Report - Edna Majaliwa
5 Sep 2019 Reviewed Reviewer Report - Suvradeep Mitra
13 Sep 2019 Author responded Author comments - Hao Liu
Resubmission - Version 2
13 Sep 2019 Submitted Manuscript version 2
20 Sep 2019 Author responded Author comments - Hao Liu
Resubmission - Version 3
20 Sep 2019 Submitted Manuscript version 3
Publishing
24 Sep 2019 Editorially accepted
9 Oct 2019 Article published 10.1186/s12887-019-1747-5

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