This article has Open Peer Review reports available.
Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient
© Morino et al.; licensee BioMed Central Ltd. 2014
Received: 6 September 2013
Accepted: 2 January 2014
Published: 7 January 2014
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 2013||Submitted||Original manuscript|
|12 Sep 2013||Author responded||Author comments - Hiroyuki Morino|
|Resubmission - Version 2|
|12 Sep 2013||Submitted||Manuscript version 2|
|8 Oct 2013||Reviewed||Reviewer Report - Daniele Ghezzi|
|15 Oct 2013||Reviewed||Reviewer Report - Filippo M. Santorelli|
|Resubmission - Version 3|
|Submitted||Manuscript version 3|
|16 Nov 2013||Author responded||Author comments - Hiroyuki Morino|
|Resubmission - Version 4|
|16 Nov 2013||Submitted||Manuscript version 4|
|19 Nov 2013||Reviewed||Reviewer Report - Daniele Ghezzi|
|20 Dec 2013||Author responded||Author comments - Hiroyuki Morino|
|Resubmission - Version 5|
|20 Dec 2013||Submitted||Manuscript version 5|
|2 Jan 2014||Editorially accepted|
|7 Jan 2014||Article published||10.1186/1471-2377-14-5|
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