|
| 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 |
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 |
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 pathway for Parkinson's Disease LRRK2 kinase to block primary cilia and Sonic hedgehog signaling in the brain.
|
30398148 |
2018 |
|
| 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 |
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 |
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 |
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 |
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 |
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 |
Comprehensive analysis of LRRK2 in publicly available Parkinson's disease cases and neurologically normal controls.
|
18213618 |
2008 |
|
| Entrez Id: |
120892 |
| Gene Symbol: |
LRRK2 |
LRRK2
|
PARKINSON DISEASE 8 (disorder)
|
0.930 |
GeneticVariation |
UNIPROT |
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease.
|
16333314 |
2006 |
|
| Entrez Id: |
120892 |
| Gene Symbol: |
LRRK2 |
LRRK2
|
PARKINSON DISEASE 8 (disorder)
|
0.930 |
GeneticVariation |
UNIPROT |
Crystal structure of the WD40 domain dimer of LRRK2.
|
30635421 |
2019 |
|
| 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 |
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 |
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 |
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 |
Interrogating Parkinson's disease LRRK2 kinase pathway activity by assessing Rab10 phosphorylation in human neutrophils.
|
29127255 |
2018 |
|
| Entrez Id: |
120892 |
| Gene Symbol: |
LRRK2 |
LRRK2
|
PARKINSON DISEASE 8 (disorder)
|
0.930 |
GeneticVariation |
UNIPROT |
Leucine-rich repeat kinase 2 regulates Sec16A at ER exit sites to allow ER-Golgi export.
|
25201882 |
2014 |
|
| 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 |
|
| 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 and Parkinsonism.
|
15811454 |
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 |
LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance.
|
16533964 |
2006 |
|
| Entrez Id: |
120892 |
| Gene Symbol: |
LRRK2 |
LRRK2
|
PARKINSON DISEASE 8 (disorder)
|
0.930 |
GeneticVariation |
UNIPROT |
Lrrk2 pathogenic substitutions in Parkinson's disease.
|
16172858 |
2005 |