Page 38 - Characterization of genetic neurodevelopmental disorders at adult age, with a focus on 22q11.2 deletion syndrome - Emma Boersma
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Figure 1. Patient characteristics and parkinsonian features in the most reported genetic disorders
*
The numerator represents how many patients were reported to present with a specific feature, and the denominator represents the number of patients with
data available.
Additional genetic mutations with potential relevance to parkinsonism were reported: a LRRK2,
b PRKN, c PRKN
Chapter 2
