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Peer Review reports

From: New mutation of the ceruloplasmin gene in the case of a neurologically asymptomatic patient with microcytic anaemia, obesity and supposed Wilson’s disease

Original Submission
7 Dec 2019 Submitted Original manuscript
21 Dec 2019 Reviewed Reviewer Report - Pietro VAJRO
29 Dec 2019 Reviewed Reviewer Report - Uta Merle
4 Jan 2020 Reviewed Reviewer Report - Ludmila Puchkova
8 Feb 2020 Author responded Author comments - Mária Ondrejkovičová
5 Mar 2020 Reviewed Reviewer Report - Pietro VAJRO
19 Mar 2020 Reviewed Reviewer Report - Ludmila Puchkova
Resubmission - Version 2
8 Feb 2020 Submitted Manuscript version 2
Publishing
25 Mar 2020 Editorially accepted
7 Apr 2020 Article published 10.1186/s12876-020-01237-8

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