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Peer Review reports

From: Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate

Original Submission
23 Mar 2016 Submitted Original manuscript
Author responded Author comments
Reviewed Reviewer Report
Resubmission - Version 2
Submitted Manuscript version 2
Author responded Author comments
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
8 Jul 2016 Editorially accepted
19 Jul 2016 Article published 10.1186/s12920-016-0208-3

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