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Mutations in XRCC1 cause cerebellar ataxia and peripheral neuropathy
Download from discovery.ucl.ac.ukFeatures of GBA-associated Parkinson’s disease at presentation in the UK Tracking Parkinson’s study
Download from research-information.bristol.ac.ukGLS loss of function causes autosomal recessive spastic ataxia and optic atrophy
Download from doi.orgEstablishing the role of rare coding variants in known Parkinson's disease risk loci
UploadPREDICT-PD: An online approach to prospectively identify risk indicators of Parkinson's disease.
Download from api.wiley.comRare variants analysis of cutaneous malignant melanoma genes in Parkinson's disease
Download from orca.cf.ac.ukLate-onset Lafora disease with prominent parkinsonism due to a rare mutation in EPM2A
Download from doi.orgA genome-wide association study in multiple system atrophy
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