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Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

Neuron · 2004 · Vol. 44(4) · pp. 601–607

Alexander Zimprich(Medical University of Vienna)Saskia BiskupPetra Leitner(University of Tübingen)Peter LichtnerMatthew J. Farrer(Mayo Clinic in Florida)Sarah Lincoln(Mayo Clinic in Florida)Jennifer M. Kachergus(Mayo Clinic in Florida)Mary Hulihan(Mayo Clinic in Florida)Ryan J. Uitti(Mayo Clinic in Florida)Donald B. Calne(University of British Columbia)A. Jon Stoessl(University of British Columbia)Ronald F. Pfeiffer(University of Tennessee Health Science Center)Nadja Patenge(Hertie Institute for Clinical Brain Research)Iria Carballo‐Carbajal(Hertie Institute for Clinical Brain Research)P. Vieregge(Klinikum Lippe)Friedrich Asmus(Hertie Institute for Clinical Brain Research)Bertram Müller‐Myhsok(Max Planck Institute of Psychiatry)Dennis W. Dickson(Mayo Clinic in Florida)Thomas Meitinger✉(Technical University of Munich)Tim M. Strom(Technical University of Munich)Zbigniew K. Wszołek✉(Mayo Clinic in Florida)Thomas Gasser✉(University of Tübingen)

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Parkinson's Disease Mechanisms and Treatments Neurological diseases and metabolism RNA regulation and diseaseParkinsonismPathologyLRRK2BiologyMedicineNeuroscienceAnatomyDiseaseParkinson's disease

MeSH terms

Leucine-Rich Repeat Serine-Threonine Protein Kinase-2Leucine-Rich Repeat ProteinsAdultAmino Acid SequenceBrainChromosome MappingFemaleHumansGenetic LinkageMaleMiddle AgedMolecular Sequence DataMutationNerve DegenerationPedigree

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