Extended Data Table 1 Clinical characteristics for carriers of the RAB32 p.S71R variant

From: Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease

  1. Individuals for which detailed case reports are available are indicated by an asterisk (Supplementary Note). ‘1’ indicates that the symptom is present, ‘0’ indicates the symptom was not present, blank indicates unknown. A ‘+’ in the Survival field indicates that the individual was alive at last follow-up. Abbreviations: PI, Parkinson Institute; AOO, age of onset; FOG, freezing of gait.
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