An atypical case of neuronal ceroid lipofuscinosis with co-inheritance of a variably penetrant POLG1mutation
© Staropoli et al.; licensee BioMed Central Ltd. 2012
Received: 29 June 2011
Accepted: 18 June 2012
Published: 24 June 2012
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting firstname.lastname@example.org.
|29 Jun 2011||Submitted||Original manuscript|
|Resubmission - Version 2|
|Submitted||Manuscript version 2|
|28 Nov 2011||Reviewed||Reviewer Report - NATALIA CANNELLI|
|19 Mar 2012||Reviewed||Reviewer Report - Filippo M. Santorelli|
|24 Mar 2012||Reviewed||Reviewer Report - Alessandro Simonati|
|17 May 2012||Author responded||Author comments - John Staropoli|
|Resubmission - Version 3|
|17 May 2012||Submitted||Manuscript version 3|
|20 May 2012||Reviewed||Reviewer Report - NATALIA CANNELLI|
|Resubmission - Version 4|
|Submitted||Manuscript version 4|
|18 Jun 2012||Editorially accepted|
|24 Jun 2012||Article published||10.1186/1471-2350-13-50|
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