A case report: autosomal recessive Myotonia congenita caused by a novel splice mutation (c.1401 + 1G > A) in CLCN1 gene of a Chinese Han patient

Peer Review reports

Original Submission
26 Jun 2018	Submitted	Original manuscript
6 Jul 2018	Reviewed	Reviewer Report - Dipa Raja Rayan
13 Jul 2018	Reviewed	Reviewer Report - Christiane Schneider-Gold
28 Jul 2018	Author responded	Author comments - Jing Miao
Resubmission - Version 2
28 Jul 2018	Submitted	Manuscript version 2
6 Aug 2018	Reviewed	Reviewer Report - Christiane Schneider-Gold
10 Sep 2018	Reviewed	Reviewer Report - Jens Reimann
Resubmission - Version 3
	Submitted	Manuscript version 3
Publishing
13 Sep 2018	Editorially accepted
22 Sep 2018	Article published	10.1186/s12883-018-1153-x

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