Implementation of a population-based epidemiological rare disease registry: study protocol of the amyotrophic lateral sclerosis (ALS) - registry Swabia
© Nagel et al.; licensee BioMed Central Ltd. 2013
Received: 2 October 2012
Accepted: 6 February 2013
Published: 17 February 2013
Open Peer Review reports
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|2 Oct 2012||Submitted||Original manuscript|
|Resubmission - Version 2|
|Submitted||Manuscript version 2|
|22 Oct 2012||Author responded||Author comments - Gabriele Nagel|
|Resubmission - Version 3|
|22 Oct 2012||Submitted||Manuscript version 3|
|14 Dec 2012||Author responded||Author comments - Gabriele Nagel|
|Resubmission - Version 4|
|14 Dec 2012||Submitted||Manuscript version 4|
|6 Feb 2013||Editorially accepted|
|17 Feb 2013||Article published||10.1186/1471-2377-13-22|
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