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Peer Review reports

From: Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death

Original Submission
24 Jan 2019 Submitted Original manuscript
15 Feb 2019 Reviewed Reviewer Report - P. Bryant Chase
22 Mar 2019 Reviewed Reviewer Report - Helena Kuivaniemi
29 Mar 2019 Reviewed Reviewer Report - Emanuela Bostjancic
25 May 2019 Author responded Author comments - Tetsuro Yokokawa
1 Jun 2019 Reviewed Reviewer Report - P. Bryant Chase
10 Jun 2019 Reviewed Reviewer Report - Helena Kuivaniemi
21 Jun 2019 Reviewed Reviewer Report - Emanuela Bostjancic
5 Jul 2019 Author responded Author comments - Tetsuro Yokokawa
Resubmission - Version 2
25 May 2019 Submitted Manuscript version 2
23 Jul 2019 Reviewed Reviewer Report - P. Bryant Chase
29 Jul 2019 Reviewed Reviewer Report - Helena Kuivaniemi
24 Aug 2019 Author responded Author comments - Tetsuro Yokokawa
Resubmission - Version 3
24 Aug 2019 Submitted Manuscript version 3
16 Oct 2019 Author responded Author comments - Tetsuro Yokokawa
Resubmission - Version 4
16 Oct 2019 Submitted Manuscript version 4
23 Nov 2019 Author responded Author comments - Tetsuro Yokokawa
Resubmission - Version 5
23 Nov 2019 Submitted Manuscript version 5
Publishing
27 Nov 2019 Editorially accepted
17 Dec 2019 Article published 10.1186/s12872-019-01282-6

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