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Peer Review reports

From: TRMA syndrome with a severe phenotype, cerebral infarction, and novel compound heterozygous SLC19A2 mutation: a case report

Original Submission
13 Mar 2019 Submitted Original manuscript
5 Jun 2019 Reviewed Reviewer Report - RB Ashokkumar
13 Jun 2019 Reviewed Reviewer Report - Agnieszka Zmyslowska
17 Jun 2019 Author responded Author comments - Xin Li
Resubmission - Version 2
17 Jun 2019 Submitted Manuscript version 2
23 Jun 2019 Author responded Author comments - Xin Li
Resubmission - Version 3
23 Jun 2019 Submitted Manuscript version 3
28 Jun 2019 Author responded Author comments - Xin Li
Resubmission - Version 4
28 Jun 2019 Submitted Manuscript version 4
Publishing
2 Jul 2019 Editorially accepted
11 Jul 2019 Article published 10.1186/s12887-019-1608-2

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