The results for LRRK2 show that several rare and common genetic variants in the same gene can have independent effects on disease risk.
Aug 31, 2011 · The results for LRRK2 show that several rare and common genetic variants in the same gene can have independent effects on disease risk.
Background The leucine-rich repeat kinase 2 gene (LRRK2) harbours highly penetrant mutations that are linked to familial parkinsonism.
Aug 30, 2011 · Pathogenic LRRK2 variability has been identified by sequencing of probands with familial parkinsonism, with results confirmed and occasionally ...
Summary Background Background The leucine-rich repeat kinase 2 gene ( LRRK2 ) harbours highly penetrant mutations that are linked to familial parkinsonism.
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: A case-control study. Owen A. Ross*, Alexandra I. Soto-Ortolaza, Michael G ...
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case- control study. In: Lancet neurology, 2011, vol. 10, n° 10, p. 898 ...
Dive into the research topics of 'Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: A case-control study'. Together they form ...
The results for LRRK2 show that several rare and common genetic variants in the same gene can have independent effects on disease risk. LRRK2, and the pathway ...
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. · The neuropathology of genetic Parkinson's ...