Skip to main content

Peer Review reports

From: A novel TAB2 nonsense mutation (p.S149X) causing autosomal dominant congenital heart defects: a case report of a Chinese family

Original Submission
17 Sep 2019 Submitted Original manuscript
18 Oct 2019 Reviewed Reviewer Report - Alexandra Frogoudaki
10 Nov 2019 Reviewed Reviewer Report - George Makavos
4 Dec 2019 Author responded Author comments - Jia Chen
24 Dec 2019 Author responded Author comments - Jia Chen
Resubmission - Version 2
4 Dec 2019 Submitted Manuscript version 2
Publishing
29 Dec 2019 Editorially accepted
20 Jan 2020 Article published 10.1186/s12872-019-01322-1

You can find further information about peer review here.

Back to article page