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Peer Review reports

From: Whole exome sequencing reveals two novel compound heterozygous mutations in TWNK as a cause of the hepatocerebral form of mitochondrial DNA depletion syndrome: a case report

Original Submission
20 Jan 2019 Submitted Original manuscript
13 Mar 2019 Reviewed Reviewer Report - Surita Meldau
21 May 2019 Reviewed Reviewer Report - Hideshi Kawakami
7 Jul 2019 Author responded Author comments - Xianghong Li
Resubmission - Version 2
7 Jul 2019 Submitted Manuscript version 2
25 Jul 2019 Author responded Author comments - Xianghong Li
Resubmission - Version 3
25 Jul 2019 Submitted Manuscript version 3
31 Jul 2019 Author responded Author comments - Xianghong Li
Resubmission - Version 4
31 Jul 2019 Submitted Manuscript version 4
5 Aug 2019 Author responded Author comments - Xianghong Li
Resubmission - Version 5
5 Aug 2019 Submitted Manuscript version 5
Publishing
11 Aug 2019 Editorially accepted
27 Aug 2019 Article published 10.1186/s12881-019-0875-y

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