1 – 6 of 6
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=""
width=""
height=""
allowtransparency="true"
frameborder="0">
</iframe>
- 2016
-
Mark
Heterozygous PINK1 p.G411S mutation increases risk for Parkinson's disease (PD)
(2016) 20th International Congress of Parkinson's Disease and Movement Disorders In Movement Disorders 31(Suppl. S2). p.282-282
- Contribution to journal › Published meeting abstract
- 2015
-
Mark
DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients.
- Contribution to journal › Article
- 2014
-
Mark
Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease
- Contribution to journal › Article
- 2013
-
Mark
GWAS risk factors in Parkinson's disease : LRRK2 coding variation and genetic interaction with PARK16
- Contribution to journal › Article
- 2011
-
Mark
A family with parkinsonism, essential tremor, restless legs syndrome, and depression
- Contribution to journal › Article
- 2007
-
Mark
Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication.
- Contribution to journal › Article
