Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins
© Toro et al.; licensee BioMed Central Ltd. 2013
Received: 9 October 2012
Accepted: 8 March 2013
Published: 20 March 2013
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting email@example.com.
|9 Oct 2012||Submitted||Original manuscript|
|14 Nov 2012||Reviewed||Reviewer Report - Ichizo Nishino|
|19 Nov 2012||Reviewed||Reviewer Report - Peter Hackman|
|27 Nov 2012||Reviewed||Reviewer Report - Hans Goebel|
|24 Dec 2012||Author responded||Author comments - Lev Goldfarb|
|Resubmission - Version 2|
|24 Dec 2012||Submitted||Manuscript version 2|
|5 Jan 2013||Reviewed||Reviewer Report - Ichizo Nishino|
|1 Feb 2013||Author responded||Author comments - Lev Goldfarb|
|Resubmission - Version 3|
|1 Feb 2013||Submitted||Manuscript version 3|
|8 Mar 2013||Editorially accepted|
|20 Mar 2013||Article published||10.1186/1471-2377-13-29|
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Open peer review is a system where authors know who the reviewers are, and the reviewers know who the authors are. If the manuscript is accepted, the named reviewer reports are published alongside the article. Pre-publication versions of the article and author comments to reviewers are available by contacting firstname.lastname@example.org. All previous versions of the manuscript and all author responses to the reviewers are also available.
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