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Peer Review reports

From: Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy

Original Submission
20 Oct 2015 Submitted Original manuscript
8 Feb 2016 Reviewed Reviewer Report - Sarah Heron
9 Feb 2016 Reviewed Reviewer Report - Radhika Dhamija
13 Feb 2016 Reviewed Reviewer Report - Santhosh Girirajan
17 Feb 2016 Reviewed Reviewer Report - Christoph Lossin
25 Mar 2016 Author responded Author comments - Andrew Fry
Resubmission - Version 2
25 Mar 2016 Submitted Manuscript version 2
Publishing
14 Apr 2016 Editorially accepted
26 Apr 2016 Article published 10.1186/s12881-016-0294-2

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BMC Medical Genetics

ISSN: 1471-2350

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