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Peer Review reports

From: A rare case of adult-onset vanishing white matter leukoencephalopathy with movement disorder, expressing homozygous EIF2B3 and PRKN pathogenic variants

Original Submission
10 Oct 2024 Submitted Original manuscript
30 Oct 2024 Reviewed Reviewer Report
25 Nov 2024 Reviewed Reviewer Report
29 Nov 2024 Author responded Author comments - Bashar Kamal Ali Douden
Resubmission - Version 2
29 Nov 2024 Submitted Manuscript version 2
2 Dec 2024 Author responded Author comments - Bashar Kamal Ali Douden
Resubmission - Version 3
2 Dec 2024 Submitted Manuscript version 3
5 Dec 2024 Reviewed Reviewer Report
27 Dec 2024 Reviewed Reviewer Report
Resubmission - Version 4
Submitted Manuscript version 4
Publishing
31 Dec 2024 Editorially accepted
4 Jan 2025 Article published 10.1186/s12883-024-04018-y

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