Skip to main content

Peer Review reports

From: Compound heterozygous c.598_612del and c.1746-20C > G CAPN3 genotype cause autosomal recessive limb-girdle muscular dystrophy-1: a case report

Original Submission
7 May 2021 Submitted Original manuscript
9 Jun 2021 Reviewed Reviewer Report
4 Jul 2021 Reviewed Reviewer Report
12 Jul 2021 Reviewed Reviewer Report
25 Aug 2021 Author responded Author comments - Evelina Siavrienė
Resubmission - Version 2
25 Aug 2021 Submitted Manuscript version 2
21 Sep 2021 Reviewed Reviewer Report
4 Oct 2021 Reviewed Reviewer Report
8 Oct 2021 Reviewed Reviewer Report
21 Oct 2021 Author responded Author comments - Evelina Siavrienė
Resubmission - Version 3
21 Oct 2021 Submitted Manuscript version 3
1 Nov 2021 Reviewed Reviewer Report
11 Nov 2021 Reviewed Reviewer Report
19 Nov 2021 Author responded Author comments - Evelina Siavrienė
Resubmission - Version 4
19 Nov 2021 Submitted Manuscript version 4
Publishing
28 Nov 2021 Editorially accepted
4 Dec 2021 Article published 10.1186/s12891-021-04920-3

You can find further information about peer review here.

Back to article page