Variants within the leucine-rich repeat kinase 2 gene are recognized as the most frequent genetic cause of Parkinson's disease. Leucine-rich repeat kinase 2 variation related to disease susceptibility displays many features that reflect the nature of complex, late-onset sporadic disorders like Parkinson's disease.

Heckman, M., Soto Ortolaza, A., Aasly, J., Abahuni, N., Annesi, G., Bacon, J., et al. (2013). Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium. MOVEMENT DISORDERS, 28(12), 1740-1744 [10.1002/mds.25600].

Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium

FERRARESE, CARLO;
2013

Abstract

Variants within the leucine-rich repeat kinase 2 gene are recognized as the most frequent genetic cause of Parkinson's disease. Leucine-rich repeat kinase 2 variation related to disease susceptibility displays many features that reflect the nature of complex, late-onset sporadic disorders like Parkinson's disease.
Articolo in rivista - Articolo scientifico
genetics; Parkinson's disease; association study; LRRK2
English
2013
28
12
1740
1744
none
Heckman, M., Soto Ortolaza, A., Aasly, J., Abahuni, N., Annesi, G., Bacon, J., et al. (2013). Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium. MOVEMENT DISORDERS, 28(12), 1740-1744 [10.1002/mds.25600].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/48214
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