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Peer Review reports

From: A rare case of a male child with post-zygotic de novo mosaic variant c.538C > T in MECP2 gene: a case report of Rett syndrome

Original Submission
2 Oct 2021 Submitted Original manuscript
15 Oct 2021 Reviewed Reviewer Report
31 Oct 2021 Reviewed Reviewer Report
10 Nov 2021 Author responded Author comments - Jhanvi Shah
Resubmission - Version 2
10 Nov 2021 Submitted Manuscript version 2
10 Nov 2021 Reviewed Reviewer Report
14 Nov 2021 Reviewed Reviewer Report
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
21 Nov 2021 Editorially accepted
2 Dec 2021 Article published 10.1186/s12883-021-02500-5

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BMC Neurology

ISSN: 1471-2377

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