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From: A novel start-loss mutation of the SLC29A3 gene in a consanguineous family with H syndrome: clinical characteristics, in silico analysis and literature review

Original Submission
4 Mar 2024 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
16 Apr 2024 Reviewed Reviewer Report
23 Apr 2024 Reviewed Reviewer Report - Stetson Thacker
12 May 2024 Reviewed Reviewer Report - Maha Hosni Morsi
27 May 2024 Author responded Author comments - Abolfazl Amini
Resubmission - Version 3
27 May 2024 Submitted Manuscript version 3
31 May 2024 Reviewed Reviewer Report - Maha Hosni Morsi
6 Jun 2024 Reviewed Reviewer Report
11 Jun 2024 Reviewed Reviewer Report - Stetson Thacker
14 Jun 2024 Author responded Author comments - Abolfazl Amini
Resubmission - Version 4
14 Jun 2024 Submitted Manuscript version 4
17 Jun 2024 Author responded Author comments - Abolfazl Amini
Resubmission - Version 5
17 Jun 2024 Submitted Manuscript version 5
24 Jun 2024 Reviewed Reviewer Report
Resubmission - Version 6
Submitted Manuscript version 6
Publishing
24 Jun 2024 Editorially accepted
4 Jul 2024 Article published 10.1186/s12920-024-01949-w

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