|
rs34637584
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.810 |
GeneticVariation
|
UNIPROT |
EFNS/MDS-ES/ENS [corrected] recommendations for the diagnosis of Parkinson's disease.
|
23279440 |
2013 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Rab29 activation of the Parkinson's disease-associated LRRK2 kinase.
|
29212815 |
2018 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Structural interface between LRRK2 and 14-3-3 protein.
|
28202711 |
2017 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Phosphorylation of amyloid precursor protein by mutant LRRK2 promotes AICD activity and neurotoxicity in Parkinson's disease.
|
28720718 |
2017 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Phosphoproteomics reveals that Parkinson's disease kinase LRRK2 regulates a subset of Rab GTPases.
|
26824392 |
2016 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
EFNS/MDS-ES/ENS [corrected] recommendations for the diagnosis of Parkinson's disease.
|
23279440 |
2013 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease.
|
22956510 |
2012 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
LRRK2 G2019S is a common mutation in Spanish patients with late-onset Parkinson's disease.
|
16298482 |
2006 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease.
|
16333314 |
2006 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance.
|
16533964 |
2006 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics.
|
16250030 |
2006 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation.
|
15929036 |
2005 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.
|
15732108 |
2005 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor.
|
16272257 |
2005 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.
|
15680455 |
2005 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
A common LRRK2 mutation in idiopathic Parkinson's disease.
|
15680457 |
2005 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
LRRK2 mutations in Parkinson disease.
|
16157908 |
2005 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.
|
16251215 |
2005 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Clinical features of LRRK2-associated Parkinson's disease in central Norway.
|
15852371 |
2005 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
G2019S LRRK2 mutation in French and North African families with Parkinson's disease.
|
16240353 |
2005 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.
|
15726496 |
2005 |
|
rs33939927
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
|
15541309 |
2004 |
|
rs34805604
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Rab29 activation of the Parkinson's disease-associated LRRK2 kinase.
|
29212815 |
2018 |
|
rs34805604
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Structural interface between LRRK2 and 14-3-3 protein.
|
28202711 |
2017 |
|
rs34805604
|
|
PARKINSON DISEASE 8 (disorder)
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Phosphorylation of amyloid precursor protein by mutant LRRK2 promotes AICD activity and neurotoxicity in Parkinson's disease.
|
28720718 |
2017 |