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Peer Review reports

From: A novel homozygous splice site variant in ARL2BP causes a syndromic autosomal recessive rod-cone dystrophy with situs inversus, asthenozoospermia, unilateral renal agenesis and microcysts

Original Submission
9 Nov 2023 Submitted Original manuscript
20 Mar 2024 Reviewed Reviewer Report
28 Mar 2024 Author responded Author comments - Paolo Enrico Maltese
Resubmission - Version 2
28 Mar 2024 Submitted Manuscript version 2
Publishing
8 Apr 2024 Editorially accepted
22 Apr 2024 Article published 10.1186/s12920-024-01868-w

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