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Peer Review reports

From: A novel splice site indel alteration in the EIF2AK3 gene is responsible for the first cases of Wolcott-Rallison syndrome in Hungary

Original Submission
4 Nov 2019 Submitted Original manuscript
3 Dec 2019 Author responded Author comments - Andrea Sümegi
31 Dec 2019 Reviewed Reviewer Report - Asma Deeb
9 Jan 2020 Reviewed Reviewer Report - Ghada M. H. Abdel-Salam
22 Jan 2020 Author responded Author comments - Andrea Sümegi
Resubmission - Version 2
3 Dec 2019 Submitted Manuscript version 2
31 Jan 2020 Author responded Author comments - Andrea Sümegi
Resubmission - Version 3
31 Jan 2020 Submitted Manuscript version 3
21 Feb 2020 Author responded Author comments - Andrea Sümegi
Resubmission - Version 4
21 Feb 2020 Submitted Manuscript version 4
Publishing
25 Feb 2020 Editorially accepted
27 Mar 2020 Article published 10.1186/s12881-020-0985-6

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