Associated Papers
An update on the monogenic causes of Parkinson's disease: Impact on patient stratification and personalised medicine.
Asmi S et al.
Ageing Research Reviews, 2026
Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects.
Periquet M et al.
American Journal of Human Genetics, 2001
Familial Parkinson's disease. Alpha-synuclein and parkin.
Mizuno Y et al.
Advances in Neurology, 2001
Progress in the clinical and molecular genetics of familial parkinsonism.
Kitada T et al.
Neurogenetics, 2000
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
Abbas N et al.
Human Molecular Genetics, 1999
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