## Abstract Parkinson's disease (PD) is characterized by progressive dopaminergic neuronal loss in the substantia nigra. The recent discovery of __leucine‐rich‐repeat kinase 2__ gene (__LRRK2__) mutations in PD is significant because these mutations are the most common cause of autosomal dominant P
✦ LIBER ✦
Molecular basis of Parkinsons’s disease linked toLRRK2mutations
✍ Scribed by Pchelina, S. N.; Emelyanov, A. K.; Usenko, T. S.
- Book ID
- 121541503
- Publisher
- SP MAIK Nauka/Interperiodica
- Year
- 2014
- Tongue
- English
- Weight
- 266 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0026-8933
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