Entrez Id: |
120892 |
Gene Symbol: |
LRRK2 |
LRRK2
|
PARKINSON DISEASE 8 (disorder)
|
0.930 |
Biomarker |
GENOMICS_ENGLAND |
|
|
|
Entrez Id: |
120892 |
Gene Symbol: |
LRRK2 |
LRRK2
|
PARKINSON DISEASE 8 (disorder)
|
0.930 |
Biomarker |
CTD_human |
|
|
|
Entrez Id: |
120892 |
Gene Symbol: |
LRRK2 |
LRRK2
|
PARKINSON DISEASE 8 (disorder)
|
0.930 |
Biomarker |
GENOMICS_ENGLAND |
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 |
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 |