LRRK2 mutations and Parkinsonism
- 1 April 2005
- journal article
- Published by Elsevier BV in The Lancet
- Vol. 365 (9466), 1230
- https://doi.org/10.1016/s0140-6736(05)74810-8
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's diseaseThe Lancet, 2005
- Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic PathologyNeuron, 2004
- Regulation of Protein Kinases: Controlling Activity through Activation Segment ConformationMolecular Cell, 2004