A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report
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* Corresponding author: Ramón A Juste rjuste@neiker.net
BMC Neurology 2010, 10:99 doi:10.1186/1471-2377-10-99
Pre-publication versions of this article and reviewers' reports
| Original Submission - Version 1 | Manuscript | 02 Oct 2009 | |
| Reviewer's Report | Pierluigi Gambetti | 13 Nov 2009 | |
| Reviewer's Report | Steven Collins | 16 Nov 2009 | |
| Resubmission - Version 2 | Manuscript | Author's comment | 10 Feb 2010 |
| Reviewer's Report | Steven Collins | 15 Apr 2010 | |
| Reviewer's Report | Pierluigi Gambetti | 25 Apr 2010 | |
| Resubmission - Version 3 | Manuscript | Author's comment | 25 Jun 2010 |
| Reviewer's Report | Steven Collins | 03 Aug 2010 | |
| Reviewer's Report | Pierluigi Gambetti | 05 Aug 2010 | |
| Reviewer's Report | Pierluigi Gambetti | 20 Aug 2010 | |
| Resubmission - Version 4 | Manuscript | Author's comment | 08 Oct 2010 |
| Resubmission - Version 5 | Manuscript | Author's comment | 08 Oct 2010 |
| Editorial acceptance | 12 Oct 2010 | ||
| Published | 25 Oct 2010 |