Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease, Neuron, vol.44, issue.4, pp.595-600, 2004. ,
DOI : 10.1016/j.neuron.2004.10.023
Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology, Neuron, vol.44, issue.4, pp.601-608, 2004. ,
DOI : 10.1016/j.neuron.2004.11.005
URL : https://doi.org/10.1016/j.neuron.2004.11.005
Cellular effects of LRRK2 mutations, Biochemical Society Transactions, vol.18, issue.5, pp.1070-1073, 2012. ,
DOI : 10.1111/j.1469-185X.2009.00082.x
URL : http://www.biochemsoctrans.org/content/ppbiost/40/5/1070.full.pdf
Heterogeneity of Leucine-Rich Repeat Kinase 2 Mutations: Genetics, Mechanisms and Therapeutic Implications, Neurotherapeutics, vol.70, issue.Suppl. 3, pp.738-50, 2014. ,
DOI : 10.1007/s00018-012-1061-y
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391379/pdf
LRRK2 in Parkinson's disease: protein domains and functional insights, Trends in Neurosciences, vol.29, issue.5, pp.286-93, 2006. ,
DOI : 10.1016/j.tins.2006.03.006
Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: A systematic review, Parkinsonism & Related Disorders, vol.16, issue.4, pp.237-279, 2010. ,
DOI : 10.1016/j.parkreldis.2009.11.004
LRRK2 Haplotype Analyses in European and North African Families with Parkinson Disease: A Common Founder for the G2019S Mutation Dating from the 13th Century, The American Journal of Human Genetics, vol.77, issue.2, pp.330-332, 2005. ,
DOI : 10.1086/432422
SNP Genotyping: The KASP Assay, Methods Mol Biology, vol.1145, pp.75-86, 2014. ,
DOI : 10.1007/978-1-4939-0446-4_7
A simple salting out procedure for extracting DNA from human nucleated cells, Nucleic Acids Research, vol.16, issue.3, p.1215, 1988. ,
DOI : 10.1093/nar/16.3.1215
URL : https://academic.oup.com/nar/article-pdf/16/3/1215/4063153/16-3-1215.pdf
Gene in Southwest European, North African, and Sephardic Jewish Subjects, Genetic Testing, vol.12, issue.3, pp.333-342, 2008. ,
DOI : 10.1089/gte.2007.0098
Clinicogenetic study of mutations inLRRK2 exon 41 in Parkinson's disease patients from 18 countries, Movement Disorders, vol.104, issue.8, pp.1102-1110, 2006. ,
DOI : 10.1212/01.WNL.0000125015.06989.DB
G2019S LRRK2 mutation in French and North African families with Parkinson's disease, Annals of Neurology, vol.77, issue.5, pp.784-791, 2005. ,
DOI : 10.1016/S0140-6736(05)17829-5
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families, Movement Disorders, vol.65, issue.1, pp.55-61, 2007. ,
DOI : 10.1017/S0317167100000068
A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease, Parkinsonism & Related Disorders, vol.14, issue.1, pp.77-80, 2008. ,
DOI : 10.1016/j.parkreldis.2007.02.001
LRRK2 Gly2019Ser penetrance in Arab???Berber patients from Tunisia: a case-control genetic study, The Lancet Neurology, vol.7, issue.7, pp.591-595, 2008. ,
DOI : 10.1016/S1474-4422(08)70116-9
A comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism, Neurobiology of Aging, vol.35, issue.5, pp.1125-1156, 2014. ,
DOI : 10.1016/j.neurobiolaging.2013.11.015
Introduction of high throughput and cost effective SNP genotyping platforms in soybean, Plant Genet Genomics Biotechnol, vol.1, issue.3, pp.90-94, 2014. ,
Comparison of custom designed KASP and TaqMan genotyping assays for a rare genetic variant identifed through resequencing GWAS loci. LGC, University of Nottingham -app note:2014. https://www.lgcgroup.com ,
Fine mapping and resequencing of the PARK16 locus in Parkinson???s disease, Journal of Human Genetics, vol.2, issue.7, pp.357-62, 2015. ,
DOI : 10.1038/nn.3801
Variants in the 3???UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expression, European Journal of Human Genetics, vol.7, issue.12, pp.1265-1274, 2012. ,
DOI : 10.1093/hmg/ddq469
EIF4G1 R1205H and VPS35 D620N mutations are rare in Parkinson's disease from South Africa, Neurobiology of Aging, vol.35, issue.2, pp.445-441, 2014. ,
DOI : 10.1016/j.neurobiolaging.2013.08.023
Missense variant in TREML2 protects against Alzheimer's disease, Neurobiology of Aging, vol.35, issue.6, pp.1510-1519, 2014. ,
DOI : 10.1016/j.neurobiolaging.2013.12.010
URL : https://doi.org/10.1016/j.neurobiolaging.2013.12.010
Late-onset Alzheimer disease risk variants mark brain regulatory loci, Neurology Genetics, vol.1, issue.2, p.15, 2015. ,
DOI : 10.1212/NXG.0000000000000012
URL : https://doi.org/10.1212/nxg.0000000000000012
Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource, Genome Research, vol.35, issue.1, pp.165-73, 2017. ,
DOI : 10.1016/j.ajhg.2011.05.029
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis, Human Molecular Genetics, vol.23, issue.8, pp.2220-2251, 2014. ,
DOI : 10.1093/hmg/ddt587
Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies, Lancet Neurol, vol.13, issue.9, pp.893-903, 2014. ,
DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases, Annals of Neurology, vol.137, issue.pt 2, pp.983-90, 2016. ,
DOI : 10.1002/ijc.28940
URL : https://hal.archives-ouvertes.fr/hal-01313687