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Subtle mutations in the SMN1 gene in Chinese patients with SMA: p.Arg288Met mutation causing SMN1 transcript exclusion of exon7

  • Qu Yu-jin1,
  • Du Juan1,
  • Li Er-zhen2,
  • Bai Jin-li1,
  • Jin Yu-wei1,
  • Wang Hong1 and
  • Song Fang1Email author
BMC Medical Genetics201213:86

DOI: 10.1186/1471-2350-13-86

Received: 9 March 2012

Accepted: 14 September 2012

Published: 20 September 2012

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Open Peer Review reports

Pre-publication versions of this article and author comments to reviewers are available by contacting info@biomedcentral.com.

Original Submission
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
Publishing
14 Sep 2012 Editorially accepted
20 Sep 2012 Article published 10.1186/1471-2350-13-86

How does Open Peer Review work?

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.. All previous versions of the manuscript and all author responses to the reviewers are also available.

You can find further information about the peer review system here.

Authors’ Affiliations

(1)
Department of Medical Genetics, Capital Institute of Pediatrics
(2)
Department of Neurology, Children’s Hospital Affiliated Capital Institute of Pediatrics

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