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Peer review reports

From: Cortical atrophy and hypofibrinogenemia due to FGG and TBCD mutations in a single family: a case report

Original Submission
29 Nov 2017 Submitted Original manuscript
28 Jan 2018 Reviewed Reviewer Report - Sulman Basit
26 Feb 2018 Reviewed Reviewer Report - Meenal Agarwal
2 Apr 2018 Author responded Author comments - Joshi Stephen
Resubmission - Version 2
2 Apr 2018 Submitted Manuscript version 2
27 Apr 2018 Author responded Author comments - Joshi Stephen
Resubmission - Version 3
27 Apr 2018 Submitted Manuscript version 3
Publishing
1 May 2018 Editorially accepted
16 May 2018 Article published 10.1186/s12881-018-0597-6

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