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Novel RAB39B loss-of-function mutation in patient with typical early-onset Parkinson's disease
Jessie R Jacobson1, Capucine Piat1, Allen J Aksamit1
1Department of Neurology, Mayo Clinic, Rochester, MN, USA.
Abstract:
RAB39B mutations have been identified in X-linked developmental delays. Recently, RAB39B mutations were identified in males with early-onset parkinsonism and intellectual disability. A novel loss-of-function RAB39B mutation was found in a female patient with typical early-onset Parkinson's disease (EOPD). RAB39B mutations may cause EOPD, potentially due to a-synuclein homeostasis disruption.
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