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Clinical Trial Summary

Parkinson's disease is a frequent neurodegenerative disorder. Genetic forms of the disease have been recently identified. The monogenic form due to parkin mutation is responsible for many familial cases and sporadic forms. However, the relationship between the mutation and the genotype of patients is not fully established. The aim of this study is to compare clinical, metabolic and neuropsychological characteristics obtained in patients with parkin mutation with those of patients without parkin mutation.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT00169364
Study type Interventional
Source Groupe Hospitalier Pitie-Salpetriere
Contact Alexis Brice, MD, PhD
Phone 33-142162183
Email brice@ccr.jussieu.fr
Status Recruiting
Phase N/A
Start date May 2002

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