Screening of WT1 mutations in exon 8 and 9 in children with steroid resistant nephrotic syndrome from a single centre and establishment of a rapid screening assay using high-resolution melting analysis in a clinical setting

Peer Review reports

Original Submission
4 Feb 2016	Submitted	Original manuscript
28 Jul 2016	Reviewed	Reviewer Report - Frederick J. Kaskel
30 Aug 2016	Reviewed	Reviewer Report - Beata S. Lipska
9 Nov 2016	Author responded	Author comments - Annes Siji
Resubmission - Version 2
9 Nov 2016	Submitted	Manuscript version 2
26 Nov 2016	Reviewed	Reviewer Report - Beata S. Lipska
8 Dec 2016	Author responded	Author comments - Annes Siji
Resubmission - Version 3
8 Dec 2016	Submitted	Manuscript version 3
Publishing
8 Dec 2016	Editorially accepted
10 Jan 2017	Article published	10.1186/s12881-016-0362-7

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