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Peer Review reports

From: Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation

Original Submission
23 May 2018 Submitted Original manuscript
29 Jun 2018 Reviewed Reviewer Report - David A Buchner
22 Aug 2018 Author responded Author comments - Jiaping Wang
Resubmission - Version 2
22 Aug 2018 Submitted Manuscript version 2
25 Sep 2018 Author responded Author comments - Jiaping Wang
Resubmission - Version 3
25 Sep 2018 Submitted Manuscript version 3
Publishing
26 Sep 2018 Editorially accepted
30 Oct 2018 Article published 10.1186/s12881-018-0699-1

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BMC Medical Genetics

ISSN: 1471-2350

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