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SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy
Download from api.wiley.comDe Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions
Download from openaccess.sgul.ac.ukA method to exploit the structure of genetic ancestry space to enhance case-control studies
Download from doi.orgSingle-molecule imaging of individual amyloid protein aggregates in human biofluids
Download from www.ncbi.nlm.nih.govKinetic model of the aggregation of alpha-synuclein provides insights into prion-like spreading
Download from doi.orgHeterogeneity in clinical features and disease severity in ataxia-associated SYNE1 mutations
Download from link.springer.comCalcium is a key factor in α-synuclein induced neurotoxicity
Download from journals.biologists.comGenetic and phenotypic characterization of complex hereditary spastic paraplegia
Download from doi.orgVariation in recent onset Parkinson’s disease: implications for pre-motor detection
Download from www.researchgate.netCHCHD2 and Parkinson's disease
Download from www.researchgate.netADCY5 mutations are another cause of benign hereditary chorea
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