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Peer Review reports

From: Diagnostic journey and genetic analysis of a novel homozygous CYP2U1 mutation causing autosomal recessive spastic paraplegia type 56 (SPG56) in a consanguineous family

Original Submission
16 Dec 2024 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
Resubmission - Version 3
Submitted Manuscript version 3
2 Jan 2025 Author responded Author comments - Jie-wei Luo
Resubmission - Version 4
2 Jan 2025 Submitted Manuscript version 4
3 Jan 2025 Author responded Author comments - Jie-wei Luo
Resubmission - Version 5
3 Jan 2025 Submitted Manuscript version 5
19 Jan 2025 Reviewed Reviewer Report
27 Jan 2025 Reviewed Reviewer Report
8 Feb 2025 Author responded Author comments - Jie-wei Luo
Resubmission - Version 6
8 Feb 2025 Submitted Manuscript version 6
12 Feb 2025 Author responded Author comments - Jie-wei Luo
Resubmission - Version 7
12 Feb 2025 Submitted Manuscript version 7
24 Feb 2025 Reviewed Reviewer Report
Resubmission - Version 8
Submitted Manuscript version 8
Publishing
28 Apr 2025 Editorially accepted
15 May 2025 Article published 10.1186/s12883-025-04211-7

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