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A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohort

Patrick Weydt*, Selma M Soyal, G Bernhard Landwehrmeyer, Wolfgang Patsch and For the European Huntington Disease Network

BMC Neurology 2014, 14:1  doi:10.1186/1471-2377-14-1

Pre-publication versions of this article and reviewers' reports

Original Submission - Version 1 08 Sep 2013
Resubmission - Version 2 Manuscript Author's comment 17 Sep 2013
Resubmission - Version 3 Manuscript Author's comment 28 Nov 2013
Editorial acceptance 10 Dec 2013
Published 02 Jan 2014