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Open Access Pre-publication history

SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis

Guillaume Rousseau, Tetsuro Noguchi, Violaine Bourdon, Hagay Sobol and Sylviane Olschwang*

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 D Gareth Evans 11 Nov 2010
Resubmission - Version 2 Manuscript Author's comment 30 Nov 2010
Reviewer's Report D 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