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Peer Review reports

From: Neutral lipid storage disease with myopathy and myotonia associated to pathogenic variants on PNPLA2 and CLCN1 genes: case report

Original Submission
16 Jan 2023 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
27 Feb 2023 Reviewed Reviewer Report
2 Mar 2023 Reviewed Reviewer Report
16 Mar 2023 Author responded Author comments - João Igor Dantas Landim
Resubmission - Version 3
16 Mar 2023 Submitted Manuscript version 3
21 Mar 2023 Author responded Author comments - João Igor Dantas Landim
Resubmission - Version 4
21 Mar 2023 Submitted Manuscript version 4
27 Mar 2023 Reviewed Reviewer Report
30 Mar 2023 Reviewed Reviewer Report
Resubmission - Version 5
Submitted Manuscript version 5
Publishing
30 Mar 2023 Editorially accepted
27 Apr 2023 Article published 10.1186/s12883-023-03195-6

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