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Peer Review reports

From: A case report of an intermediate phenotype between congenital myasthenic syndrome and D-2- and L-2-hydroxyglutaric aciduria due to novel SLC25A1 variants

Original Submission
16 Apr 2020 Submitted Original manuscript
23 Apr 2020 Author responded Author comments - Wenhui Li
Resubmission - Version 2
23 Apr 2020 Submitted Manuscript version 2
14 May 2020 Reviewed Reviewer Report
24 May 2020 Reviewed Reviewer Report - Carmelo Rodolico
19 Jun 2020 Author responded Author comments - Wenhui Li
Resubmission - Version 3
19 Jun 2020 Submitted Manuscript version 3
29 Jun 2020 Author responded Author comments - Wenhui Li
Resubmission - Version 4
29 Jun 2020 Submitted Manuscript version 4
Publishing
2 Jul 2020 Editorially accepted
13 Jul 2020 Article published 10.1186/s12883-020-01854-6

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