Open Access Pre-publication history

Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disorders

Clare N Lynex*, Ian M Carr, Jack P Leek, Rajgopal Achuthan, Simon Mitchell, Eamonn R Maher, C Geoffrey Woods, David T Bonthon and Alex F Markham

BMC Neurology 2004, 4:20 doi:10.1186/1471-2377-4-20

Pre-publication versions of this article and reviewers' reports

Original Submission - Version 1 Manuscript 05 May 2004
Reviewer's Report Hans-Michael Meinck 30 Jun 2004
Reviewer's Report lisbeth tranebjaerg 28 Jul 2004
Resubmission - Version 2 Manuscript Author's comment 16 Oct 2004
Reviewer's Report lisbeth tranebjaerg 04 Nov 2004
Reviewer's Report Hans-Michael Meinck 11 Nov 2004
Resubmission - Version 3 Manuscript Author's comment 22 Nov 2004
Resubmission - Version 4 Manuscript 26 Nov 2004
Published 30 Nov 2004