×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease.
15541308
2004
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
15541309
2004
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.
15680455
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.
15680456
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
A common LRRK2 mutation in idiopathic Parkinson's disease.
15680457
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.
15726496
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.
15732108
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
LRRK2 mutations and Parkinsonism.
15811454
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Clinical features of LRRK2-associated Parkinson's disease in central Norway.
15852371
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family.
15880653
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
LRRK2 R1441G in Spanish patients with Parkinson's disease.
15925109
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation.
15929036
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Clinical traits of LRRK2-associated Parkinson's disease in Ireland: a link between familial and idiopathic PD.
16102999
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
LRRK2 gene in Parkinson disease: mutation analysis and case control association study.
16157901
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
LRRK2 mutations in Parkinson disease.
16157908
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations.
16157909
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Lrrk2 pathogenic substitutions in Parkinson's disease.
16172858
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
G2019S LRRK2 mutation in French and North African families with Parkinson's disease.
16240353
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Analysis of LRRK2 functional domains in nondominant Parkinson disease.
16247070
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics.
16250030
2006
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.
16251215
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity.
16269541
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data.
16272164
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
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
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
LRRK2 G2019S is a common mutation in Spanish patients with late-onset Parkinson's disease.
16298482
2006