Publication | Open Access

Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations

Molecular NeuroscienceMendelian DisorderGenetic DisorderGeneticsParkinson DiseaseAutosomal Dominant ParkinsonismCommon FounderSystems BiologyMedicineNovel Lrrk2 Mutation