Harhangi, B.S.

disease study parkinson patient family mutation allele dementia genotype control parkinsonism rotterdam frequency association rotterdam study tumor population result ziekte van parkinson susceptibility parkin onset table parkin gene polymorphism analysis factor autosomal apoe genotype linkage cyp 2d gene european ziekte region context link chromosome pd patients family history cause recessive diagnosis individual neurology epsilon neurol deletion alzheimer marker history european consortium sample chapter number genet type allele participant hemangioblastoma protein apolipoprotein cohort nat -2 gene seizure acetylator system person point finding group disorder baseline genotyping sib pairs subject evidence nat -2 polymorphism aggregation context intracranial ees /ppnet uch-ll gene cyp 2d