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
© Lynex et al; licensee BioMed Central Ltd. 2004
Received: 05 May 2004
Accepted: 30 November 2004
Published: 30 November 2004
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting firstname.lastname@example.org.
|5 May 2004||Submitted||Original manuscript|
|Resubmission - Version 2|
|Submitted||Manuscript version 2|
|30 Jun 2004||Reviewed||Reviewer Report - Hans-Michael Meinck|
|28 Jul 2004||Reviewed||Reviewer Report - Lisbeth Tranebjaerg|
|16 Oct 2004||Author responded||Author comments - Clare Lynex|
|Resubmission - Version 3|
|16 Oct 2004||Submitted||Manuscript version 3|
|4 Nov 2004||Reviewed||Reviewer Report - Lisbeth Tranebjaerg|
|11 Nov 2004||Reviewed||Reviewer Report - Hans-Michael Meinck|
|22 Nov 2004||Author responded||Author comments - Clare Lynex|
|Resubmission - Version 4|
|22 Nov 2004||Submitted||Manuscript version 4|
|30 Nov 2004||Editorially accepted|
|30 Nov 2004||Article published||10.1186/1471-2377-4-20|
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