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

Peer Review reports

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
Publishing
30 Jul 2018	Editorially accepted
25 Sep 2018	Article published	10.1186/s13256-018-1788-7

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