Dr Kishore Kumar
NHMRC
Australia
Investigating the clinical and research applications of whole-genome sequencing in Parkinson disease and other movement disorders
NHMRC
177,160
01/01/15
4.0
Parkinson's disease & PD-related disorders
neurology | neurogenetics | genetics | parkinson disease | dystonia
There are many movement disorders including Parkinson disease, dystonia, and hereditary spastic paraplegia. These disorders can be caused by mutations (errors in the genetic code) in different genes. The discovery of these genes has improved our understanding of the underlying disease mechanisms. We will use whole genome sequencing to read a persons entire genetic material in a single experiment, allowing us to identify a genetic diagnosis and to discover entirely new disease-causing genes.