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Peer Review reports

From: An insertion mutation of the MECP2 gene in severe neonatal encephalopathy and ocular and oropharyngeal dyskinesia: a case report

Original Submission
8 Jan 2023 Submitted Original manuscript
10 Apr 2023 Reviewed Reviewer Report
23 Jun 2023 Reviewed Reviewer Report
13 Jul 2023 Author responded Author comments - Xuemei Wu
Resubmission - Version 2
13 Jul 2023 Submitted Manuscript version 2
26 Jul 2023 Editorially accepted
3 Aug 2023 Article published 10.1186/s12920-023-01616-6

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