Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia

Peer Review reports

Original Submission
8 Oct 2023	Submitted	Original manuscript
30 Nov 2023	Reviewed	Reviewer Report
29 May 2024	Reviewed	Reviewer Report
13 Jun 2024	Author responded	Author comments - Mohammad Amin Tabatabaiefar
14 Jun 2024	Author responded	Author comments - Mohammad Amin Tabatabaiefar
Resubmission - Version 2
13 Jun 2024	Submitted	Manuscript version 2
19 Jun 2024	Reviewed	Reviewer Report
Resubmission - Version 3
	Submitted	Manuscript version 3
Publishing
19 Jun 2024	Editorially accepted
1 Jul 2024	Article published	10.1186/s12920-024-01942-3

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