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Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.How much phenotypic variation can be attributed to parkin genotype?G51D α-synuclein mutation causes a novel parkinsonian-pyramidal syndrome.The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism.A multidisciplinary study of patients with early-onset PD with and without parkin mutations.Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?G2019S LRRK2 mutation in French and North African families with Parkinson's disease.LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans.Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease.LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century.Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.Young-onset Parkinson disease with and without parkin gene mutations: a fluorodopa F 18 positron emission tomography study.A multitracer dopaminergic PET study of young-onset parkinsonian patients with and without parkin gene mutations.Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease.A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations.Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms.Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease.Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease.EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?Parkin mutations are frequent in patients with isolated early-onset parkinsonism.New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism.
P50
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P50
name
French Parkinson's Disease Genetics Study Group
@en
type
label
French Parkinson's Disease Genetics Study Group
@en
prefLabel
French Parkinson's Disease Genetics Study Group
@en