This article has Open Peer Review reports available.
Atypical case of Wolfram syndrome revealed through targeted exome sequencing in a patient with suspected mitochondrial disease
- Daniel S Lieber†1, 2, 3, 4,
- Scott B Vafai†1, 2, 3, 4, 5,
- Laura C Horton6,
- Nancy G Slate1, 2,
- Shangtao Liu1, 2,
- Mark L Borowsky1, 4,
- Sarah E Calvo1, 2, 3, 4,
- Jeremy D Schmahmann6Email author and
- Vamsi K Mootha1, 2, 3, 4Email author
© Lieber et al; licensee BioMed Central Ltd. 2012
Received: 6 September 2011
Accepted: 6 January 2012
Published: 6 January 2012
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting firstname.lastname@example.org.
|6 Sep 2011||Submitted||Original manuscript|
|Resubmission - Version 2|
|Submitted||Manuscript version 2|
|28 Sep 2011||Reviewed||Reviewer Report - Lisbeth Tranebjaerg|
|9 Oct 2011||Reviewed||Reviewer Report - Emna Mkaouar-Rebai|
|10 Oct 2011||Reviewed||Reviewer Report - Yukio Tanizawa|
|16 Nov 2011||Author responded||Author comments - Daniel Lieber|
|Resubmission - Version 3|
|16 Nov 2011||Submitted||Manuscript version 3|
|23 Nov 2011||Reviewed||Reviewer Report - Yukio Tanizawa|
|9 Dec 2011||Reviewed||Reviewer Report - Lisbeth Tranebjaerg|
|21 Dec 2011||Author responded||Author comments - Daniel Lieber|
|Resubmission - Version 4|
|21 Dec 2011||Submitted||Manuscript version 4|
|28 Dec 2011||Reviewed||Reviewer Report - Lisbeth Tranebjaerg|
|Resubmission - Version 5|
|Submitted||Manuscript version 5|
|6 Jan 2012||Editorially accepted|
|6 Jan 2012||Article published||10.1186/1471-2350-13-3|
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