Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review.

Mov Disord Clin Pract · 2023 · PMC9847320 · PMID 36699000

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may be significantno p-value reported

Research Implications Phenotypic heterogeneity may be significant in GNDs given incomplete penetrance of genetic variants, variable expression, and pleiotropy, 43 and may be particularly relevant in those GNDs involving multiple genes, such as is the case in 22q11.2 deletion syndrome.

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