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Peer Review reports

From: Hereditary pheochromocytoma/paraganglioma syndrome with a novel mutation in the succinate dehydrogenase subunit B gene in a Japanese family: two case reports

Original Submission
14 Dec 2020 Submitted Original manuscript
3 Mar 2021 Reviewed Reviewer Report - Otabek Yangibaev
5 Mar 2021 Reviewed Reviewer Report - Venu Madhav Chippa
23 Mar 2021 Author responded Author comments - Rei Hirose
Resubmission - Version 2
23 Mar 2021 Submitted Manuscript version 2
24 Mar 2021 Reviewed Reviewer Report - Venu Madhav Chippa
4 Apr 2021 Reviewed Reviewer Report - Ho Gwo Fuang
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
5 Apr 2021 Editorially accepted
22 May 2021 Article published 10.1186/s13256-021-02852-z

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Journal of Medical Case Reports

ISSN: 1752-1947