Pre-publication history
SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis
BMC Neurology 2011, 11:9 doi:10.1186/1471-2377-11-9
Pre-publication versions of this article and reviewers' reports
| Original Submission - Version 1 | Manuscript | 07 Oct 2010 | |
| Reviewer's Report | paul brennan | 02 Nov 2010 | |
| Reviewer's Report | Gareth Evans | 11 Nov 2010 | |
| Resubmission - Version 2 | Manuscript | Author's comment | 30 Nov 2010 |
| Reviewer's Report | Gareth Evans | 22 Dec 2010 | |
| Reviewer's Report | paul brennan | 22 Dec 2010 | |
| Resubmission - Version 3 | Manuscript | Author's comment | 03 Jan 2011 |
| Resubmission - Version 4 | Manuscript | Author's comment | 14 Jan 2011 |
| Editorial acceptance | 18 Jan 2011 | ||
| Published | 24 Jan 2011 |
