LRRK2 mutations and Parkinsonism

This publication has 3 references indexed in Scilit:

• A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease
  The Lancet, 2005
• Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
  Neuron, 2004
• Regulation of Protein Kinases
  Molecular Cell, 2004