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A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findings

Naomi F Bramhall, Jeremy C Kallman, Aimee M Verrall and Valerie A Street*

BMC Medical Genetics 2008, 9:48  doi:10.1186/1471-2350-9-48

Pre-publication versions of this article and reviewers' reports

Original Submission - Version 1 Manuscript 11 Dec 2007
Reviewer's Report Ronald Pennings 31 Dec 2007
Reviewer's Report Nikolaus Blin 04 Jan 2008
Reviewer's Report Marci Lesperance 10 Jan 2008
Reviewer's Report Edi Sartorato 17 Jan 2008
Resubmission - Version 2 Manuscript Author's comment 03 Apr 2008
Resubmission - Version 3 Manuscript Author's comment 03 Apr 2008
Reviewer's Report Ronald Pennings 18 Apr 2008
Reviewer's Report Nikolaus Blin 29 Apr 2008
Resubmission - Version 4 Manuscript Author's comment 13 May 2008
Editorial acceptance 27 May 2008
Published 02 Jun 2008