Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

Neuron

Volumn 44, Issue 4, 2004, Pages 601-607

  Zimprich, Alexander ^a,b   Biskup, Saskia ^c   Leitner, Petra ^a   Lichtner, Peter ^c   Farrer, Matthew ^d   Lincoln, Sarah ^d   Kachergus, Jennifer ^d   Hulihan, Mary ^d   Uitti, Ryan J ^e   Calne, Donald B ^f   Stoessl, A Jon ^f   Pfeiffer, Ronald F ^g   Patenge, Nadja ^a   Carbajal, Iria Carballo ^a   Vieregge, Peter ^h   Asmus, Friedrich ^a   Müller Myhsok, Bertram ⁱ   Dickson, Dennis W ^d   Meitinger, Thomas ^c,j   Strom, Tim M ^c,j   Wszolek, Zbigniew K ^e   Gasser, Thomas ^a   more..

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b MEDICAL UNIVERSITY OF VIENNA   (Austria)

^c INSTITUTE OF EPIDEMIOLOGY   (Germany)

^d MAYO GRADUATE SCHOOL   (United States)

^e MAYO CLINIC   (United States)

^f UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^g UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

^h KLINIKUM LIPPE DETMOLD   (Germany)

ⁱ MAX PLANCK INSTITUTE OF PSYCHIATRY   (Germany)

^j TECHNICAL UNIVERSITY OF MUNICH   (Germany)

more..

Author keywords

[No Author keywords available]

Indexed keywords

LEUCINE RICH REPEAT KINASE 2; PHOSPHOTRANSFERASE; UNCLASSIFIED DRUG;

ARTICLE; CHROMOSOME ANALYSIS; CONTROLLED STUDY; DEMENTIA; DISEASE ASSOCIATION; DOPAMINERGIC SYSTEM; GENE MUTATION; GENE SEQUENCE; GENETIC LINKAGE; HUMAN; HUMAN CELL; MISSENSE MUTATION; MUSCLE ATROPHY; NUCLEOTIDE SEQUENCE; PARKINSONISM; PATHOGENESIS; PRIORITY JOURNAL; RNA SPLICING;

EID: 8844233579     PISSN: 08966273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuron.2004.11.005     Document Type: Article

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