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FBXO7–R498X mutation: Phenotypic variability from chorea to early onset parkinsonism within a family

Early Onset ParkinsonismNeurodegenerative DiseasesMendelian DisorderGenetic DisorderGeneticsFbxo7–r498x MutationPhenotypic VariabilityDegenerative DiseaseNeurologyNeuroscienceDisease Gene IdentificationNeuropathologyMedicineMovement Disorders