Prevalence and clinical features of LRRK2 mutations in patients with Parkinson’s disease in southern Spain

Background and purpose: Mutations in leucine‐rich repeat kinase 2 (LRRK2) gene are associated with both familial and idiopathic Parkinson’s disease (PD), whereas mutations in PARK2 (PARKIN) gene result in early onset recessive PD. Here, the objectives were to determine the frequency of LRRK2 G2019S...

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Veröffentlicht in:	European journal of neurology 2009-08, Vol.16 (8), p.957-960
Hauptverfasser:	Gao, L., Gómez‐Garre, P., Díaz‐Corrales, F. J., Carrillo, F., Carballo, M., Palomino, A., Díaz‐Martín, J., Mejías, R., Vime, P. J., López‐Barneo, J., Mir, P.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Age of Onset clinical features DNA Mutational Analysis Female Gene Frequency genetic study Haplotypes Humans Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 leucine‐rich repeat kinase 2 Male Middle Aged Mutation Mutation, Missense PARKIN Parkinson Disease - genetics Parkinson’s disease Polymorphism, Genetic Protein-Serine-Threonine Kinases - genetics Sequence Deletion Ubiquitin-Protein Ligases - genetics
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