Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2
© Bras et al; licensee BioMed Central Ltd. 2008
Received: 12 June 2007
Accepted: 22 January 2008
Published: 22 January 2008
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting firstname.lastname@example.org.
|12 Jun 2007||Submitted||Original manuscript|
|9 Jul 2007||Reviewed||Reviewer Report - Hao Deng|
|12 Jul 2007||Reviewed||Reviewer Report - José Berciano|
|17 Jul 2007||Reviewed||Reviewer Report - Stefano Goldwurm|
|28 Aug 2007||Author responded||Author comments - Jose Bras|
|Resubmission - Version 2|
|28 Aug 2007||Submitted||Manuscript version 2|
|11 Sep 2007||Reviewed||Reviewer Report - Hao Deng|
|13 Sep 2007||Reviewed||Reviewer Report - Stefano Goldwurm|
|19 Nov 2007||Author responded||Author comments - Jose Bras|
|Resubmission - Version 3|
|19 Nov 2007||Submitted||Manuscript version 3|
|5 Dec 2007||Reviewed||Reviewer Report - Stefano Goldwurm|
|8 Jan 2008||Author responded||Author comments - Jose Bras|
|Resubmission - Version 4|
|8 Jan 2008||Submitted||Manuscript version 4|
|22 Jan 2008||Editorially accepted|
|22 Jan 2008||Article published||10.1186/1471-2377-8-1|
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