Skip to main content

Peer Review reports

From: Identification of a novel GLA mutation (Y88C) in a Korean family with Fabry nephropathy: a case report

Original Submission
29 Jun 2016 Submitted Original manuscript
Author responded Author comments
Reviewed Reviewer Report
Resubmission - Version 2
Submitted Manuscript version 2
Author responded Author comments
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
17 Oct 2016 Editorially accepted
24 Oct 2016 Article published 10.1186/s12881-016-0338-7

You can find further information about peer review here.

Back to article page