Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a delayed diagnosis: a case report

Peer Review reports

Original Submission
17 Oct 2017	Submitted	Original manuscript
15 Jan 2018	Author responded	Author comments - Jingru Lu
Resubmission - Version 2
15 Jan 2018	Submitted	Manuscript version 2
12 Mar 2018	Reviewed	Reviewer Report - Dominik Müller
9 Apr 2018	Reviewed	Reviewer Report - Maria Szczepanska
15 May 2018	Author responded	Author comments - Jingru Lu
Resubmission - Version 3
15 May 2018	Submitted	Manuscript version 3
6 Jun 2018	Author responded	Author comments - Jingru Lu
Resubmission - Version 4
6 Jun 2018	Submitted	Manuscript version 4
Publishing
28 Jun 2018	Editorially accepted
13 Jul 2018	Article published	10.1186/s12882-018-0979-1

Back to article page