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Peer Review reports

From: Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case report

Original Submission
6 Feb 2021 Submitted Original manuscript
16 Feb 2021 Reviewed Reviewer Report
2 Mar 2021 Reviewed Reviewer Report
24 Mar 2021 Author responded Author comments - Youssef El Kadiri
Resubmission - Version 2
24 Mar 2021 Submitted Manuscript version 2
29 Mar 2021 Reviewed Reviewer Report
31 Mar 2021 Reviewed Reviewer Report
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
12 Apr 2021 Editorially accepted
21 Apr 2021 Article published 10.1186/s12920-021-00959-2

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