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Peer Review reports

From: Hereditary spastic paraplegia and extensive leukoencephalopathy: a case report of a unique phenotype associated with a GJB1/Cx32 p.Pro174Ser variant

Original Submission
22 Jun 2024 Submitted Original manuscript
27 Jun 2024 Author responded Author comments - Fumiaki Tanaka
27 Jun 2024 Author responded Author comments - Fumiaki Tanaka
Resubmission - Version 2
27 Jun 2024 Submitted Manuscript version 2
4 Jul 2024 Author responded Author comments - Fumiaki Tanaka
Resubmission - Version 3
4 Jul 2024 Submitted Manuscript version 3
28 Jul 2024 Reviewed Reviewer Report - Teresa Sevilla
31 Jul 2024 Reviewed Reviewer Report
2 Aug 2024 Reviewed Reviewer Report
4 Aug 2024 Reviewed Reviewer Report - Quentin Thomas
21 Aug 2024 Author responded Author comments - Fumiaki Tanaka
Resubmission - Version 4
21 Aug 2024 Submitted Manuscript version 4
Publishing
26 Aug 2024 Editorially accepted
4 Sep 2024 Article published 10.1186/s12883-024-03823-9

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