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 firstname.lastname@example.org.
|9 Oct 2012||Submitted||Original manuscript|
|Resubmission - Version 2|
|Submitted||Manuscript version 2|
|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 3|
|24 Dec 2012||Submitted||Manuscript version 3|
|5 Jan 2013||Reviewed||Reviewer Report - Ichizo Nishino|
|1 Feb 2013||Author responded||Author comments - Lev Goldfarb|
|Resubmission - Version 4|
|1 Feb 2013||Submitted||Manuscript version 4|
|8 Mar 2013||Editorially accepted|
|20 Mar 2013||Article published||10.1186/1471-2377-13-29|
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