The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type V

Peer Review reports

Original Submission
12 Jul 2013	Submitted	Original manuscript
20 Sep 2013	Reviewed	Reviewer Report - Minna Mannikko
12 Dec 2013	Reviewed	Reviewer Report - Franco Antoniazzi
14 Feb 2014	Author responded	Author comments - Syndia Lazarus
Resubmission - Version 2
14 Feb 2014	Submitted	Manuscript version 2
Publishing
10 Mar 2014	Editorially accepted
27 Mar 2014	Article published	10.1186/1471-2474-15-107

Back to article page