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Peer Review reports

From: Homozygosity mapping identified a novel protein truncating mutation (p.Ser100Leufs*24) of the BBS9 gene in a consanguineous Pakistani family with Bardet Biedl syndrome

Original Submission
31 Jul 2015 Submitted Original manuscript
25 Sep 2015 Reviewed Reviewer Report - Elaine Lim
12 Oct 2015 Reviewed Reviewer Report - Diana Valverde
6 Dec 2015 Author responded Author comments - Muzammil Ahmad Khan
Resubmission - Version 2
6 Dec 2015 Submitted Manuscript version 2
11 Dec 2015 Reviewed Reviewer Report - Elaine Lim
14 Dec 2015 Reviewed Reviewer Report - Diana Valverde
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
19 Jan 2016 Editorially accepted
4 Feb 2016 Article published 10.1186/s12881-016-0271-9

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