Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations

Neurology

Volumn 71, Issue 4, 2008, Pages 303-

  Ross, Owen A ^a   Toft, Mathias ^a   Haugarvoll, Kristoffer ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

LEUCINE RICH REPEAT KINASE 2; LRRK2 PROTEIN, HUMAN; PROTEIN SERINE THREONINE KINASE;

BRAIN DISEASE; CONTROLLED STUDY; CORTICOBASAL SYNDROME; GENE IDENTIFICATION; GENE MUTATION; GENETIC VARIABILITY; HUMAN; LETTER; PARKINSON DISEASE; PATHOGENICITY; PRIMARY PROGRESSIVE APHASIA; PRIORITY JOURNAL; RISK FACTOR; DEGENERATIVE DISEASE; EPIDEMIOLOGY; GENETIC MARKER; GENETIC PREDISPOSITION; GENETIC SCREENING; GENETICS; GENOTYPE; INHERITANCE; METABOLISM; MUTATION; NORWAY; NOTE; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; STANDARD;

APHASIA, PRIMARY PROGRESSIVE; CAUSALITY; DNA MUTATIONAL ANALYSIS; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; GENOTYPE; HUMANS; INHERITANCE PATTERNS; MUTATION; NEURODEGENERATIVE DISEASES; NORWAY; PARKINSON DISEASE; PROTEIN-SERINE-THREONINE KINASES; RISK FACTORS; VARIATION (GENETICS);

EID: 50549085963     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/01.wnl.0000320511.30222.dd     Document Type: Letter

References (5)

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2. AS Chen-Plotkin W Yuan C Anderson Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations Neurology 70 2008 521 527
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5. M Toft K Haugarvoll OA Ross MJ Farrer JO Aasly LRRK2 and Parkinson's disease in Norway Acta Neurol Scand Suppl 187 2007 72 75