de Silva,Rohan

Institution: UCL Institute of Neurology, UK

Research Interests: Dementia, Disease, Frontotemporal Dementia, Gene, Chromosome, Chromosome 17, Frontotemporal Dementia With Parkinsonism, Mutations, Palsy, Parkinsonism, Progressive Supranuclear Palsy, Tauopathies, Haplotype, Risk, Exon, Microtubule, Mutation, Association, Families, Haplotypes