Deep sequencing of SMPD1 gene revealed a heterozygous frameshift mutation (p.Ser192Alafs) in a Palestinian infant with Niemann–Pick disease type A: a case report

Peer Review reports

Original Submission
10 Apr 2018	Submitted	Original manuscript
19 Jun 2018	Reviewed	Reviewer Report - Nelmar Ortiz Cabrera
26 Jun 2018	Reviewed	Reviewer Report - Walid AL ACHKAR
27 Jun 2018	Reviewed	Reviewer Report - Satomi Okano
14 Aug 2018	Author responded	Author comments - Abedelmajeed Nasereddin
Resubmission - Version 2
14 Aug 2018	Submitted	Manuscript version 2
15 Aug 2018	Reviewed	Reviewer Report - Walid AL ACHKAR
15 Aug 2018	Reviewed	Reviewer Report - Nelmar Ortiz Cabrera
Resubmission - Version 3
	Submitted	Manuscript version 3
Publishing
16 Aug 2018	Editorially accepted
18 Sep 2018	Article published	10.1186/s13256-018-1805-x

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