Novel compound heterozygous variants of the SEC23A gene in a Chinese family with cranio-lenticulo-sutural dysplasia based on data from a large cohort of congenital cataract patients

Peer Review reports

Original Submission
19 May 2023	Submitted	Original manuscript
Resubmission - Version 2
	Submitted	Manuscript version 2
Resubmission - Version 3
	Submitted	Manuscript version 3
28 Jul 2023	Reviewed	Reviewer Report - Sairah Yousaf
16 Aug 2023	Reviewed	Reviewer Report
24 Aug 2023	Reviewed	Reviewer Report
12 Sep 2023	Author responded	Author comments - Weirong Chen
Resubmission - Version 4
12 Sep 2023	Submitted	Manuscript version 4
17 Sep 2023	Reviewed	Reviewer Report
18 Sep 2023	Reviewed	Reviewer Report - Sairah Yousaf
Resubmission - Version 5
	Submitted	Manuscript version 5
Publishing
19 Sep 2023	Editorially accepted
12 Oct 2023	Article published	10.1186/s12920-023-01667-9

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