Gait alterations in healthy carriers of the LRRK2 G2019S mutation
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ana.22165/fullpdf
Reference20 articles.
1. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews;Ozelius;N Engl J Med,2006
2. Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease;Goldwurm;Neurology,2007
3. Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations;Kachergus;Am J Hum Genet,2005
4. The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect?;Orr-Urtreger;Neurology,2007
5. Marked alterations in the gait timing and rhythmicity of patients with de novo Parkinson's disease;Baltadjieva;Eur J Neurosci,2006
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