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Peer Review reports

From: A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family

Original Submission
19 Oct 2017 Submitted Original manuscript
2 Nov 2017 Author responded Author comments - Jing Miao
Resubmission - Version 2
2 Nov 2017 Submitted Manuscript version 2
1 Dec 2017 Reviewed Reviewer Report - Rudolf Kley
12 Dec 2017 Reviewed Reviewer Report - Kristl Claeys
10 Jan 2018 Author responded Author comments - Jing Miao
Resubmission - Version 3
10 Jan 2018 Submitted Manuscript version 3
11 Feb 2018 Reviewed Reviewer Report - Jens Reimann
13 Feb 2018 Reviewed Reviewer Report - Rudolf Kley
2 Mar 2018 Author responded Author comments - Jing Miao
Resubmission - Version 4
2 Mar 2018 Submitted Manuscript version 4
25 Apr 2018 Reviewed Reviewer Report - Vincenzo Sorrentino
11 May 2018 Author responded Author comments - Jing Miao
Resubmission - Version 5
11 May 2018 Submitted Manuscript version 5
Publishing
22 May 2018 Editorially accepted
4 Jun 2018 Article published 10.1186/s12883-018-1078-4

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