Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson’s disease
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Oxford University Press
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13
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Abstract
The recurrent 22q11.2 deletion is a genetic risk factor for early-onset Parkinson's disease. Adults with the associated 22q11.2 deletion syndrome (22q11.2DS) may exhibit phenotypes that could help ide...
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Brain. 2017 Mar 24
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