|
1
|
Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's disease.
|
Ann Neurol
|
2006
|
1.66
|
|
2
|
Expanding the clinical phenotype of SNCA duplication carriers.
|
Mov Disord
|
2009
|
1.25
|
|
3
|
Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries.
|
Mov Disord
|
2006
|
1.20
|
|
4
|
Mutations in the NHLRC1 gene are the common cause for Lafora disease in the Japanese population.
|
J Hum Genet
|
2005
|
0.88
|
|
5
|
A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese.
|
Hum Mol Genet
|
2011
|
0.86
|
|
6
|
Neck weakness is a potent prognostic factor in sporadic amyotrophic lateral sclerosis patients.
|
J Neurol Neurosurg Psychiatry
|
2013
|
0.83
|