Subtle mutations in the SMN1 gene in Chinese patients with SMA: p.Arg288Met mutation causing SMN1 transcript exclusion of exon7
© Qu et al.; licensee BioMed Central Ltd. 2012
Received: 9 March 2012
Accepted: 14 September 2012
Published: 20 September 2012
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting email@example.com.
|9 Mar 2012||Submitted||Original manuscript|
|Resubmission - Version 2|
|Submitted||Manuscript version 2|
|Resubmission - Version 3|
|Submitted||Manuscript version 3|
|9 Mar 2012||Author responded||Author comments - Yu-jin Qu|
|Resubmission - Version 4|
|9 Mar 2012||Submitted||Manuscript version 4|
|13 Mar 2012||Author responded||Author comments - Yu-jin Qu|
|Resubmission - Version 5|
|13 Mar 2012||Submitted||Manuscript version 5|
|3 Jun 2012||Reviewed||Reviewer Report - Francesco Danilo Tiziano|
|4 Jun 2012||Reviewed||Reviewer Report - Federica Sangiuolo|
|10 Aug 2012||Author responded||Author comments - Yu-jin Qu|
|Resubmission - Version 6|
|10 Aug 2012||Submitted||Manuscript version 6|
|14 Sep 2012||Editorially accepted|
|20 Sep 2012||Article published||10.1186/1471-2350-13-86|
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