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Peer Review reports

From: Novel in-frame deletion in MFSD8 gene revealed by trio whole exome sequencing in an Iranian affected with neuronal ceroid lipofuscinosis type 7: a case report

Original Submission
2 Oct 2017 Submitted Original manuscript
24 Dec 2017 Reviewed Reviewer Report - mansoor abdulla
25 Dec 2017 Reviewed Reviewer Report - Fuad Almutairi
20 Feb 2018 Author responded Author comments - Ali Hosseini Bereshneh
Resubmission - Version 2
20 Feb 2018 Submitted Manuscript version 2
30 Jul 2018 Editorially accepted
25 Sep 2018 Article published 10.1186/s13256-018-1788-7

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