Article

<i>RAB32</i>-linked Parkinson’s disease: Deep phenotyping, MDSGene literature review, and application of SynNeurGe criteria

2025-06-03

Abstract excerpt

<h4>Background</h4> The RAB32 p.Ser71Arg variant is a novel cause of monogenic Parkinson’s disease (PD), for which detailed phenotypic information is currently scarce. <h4>Objectives</h4> To clinically and biologically characterize individuals with PARK- RAB32 to gain insights into genotype-phenotype relationships, disease severity, and underlying pathology. <h4>Methods</h4> We conducted a literature review follow...

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Literature Corpus work: ad4a4cf1-8ea7-57fe-8278-c40e3cb652df
DOI: 10.1101/2025.06.03.25328628

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