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
The genetic architecture of Parkinson's disease on the Island of Crete.
Boura I et al.
Npj Parkinson's Disease, 2025
Genetic analysis of the LRP10 gene in Chinese patients with Parkinson's disease.
Song N et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2023
Analysis of p.Tyr307Asn variant in the LRP10 gene in Parkinson's disease in southern Spain.
Periñán MT et al.
Neurobiology of Aging, 2020
Clinical and Pathological Phenotypes of LRP10 Variant Carriers with Dementia.
Vergouw LJM et al.
Journal of Alzheimer's Disease : Jad, 2020
Mutation analysis of LRP10 in Japanese patients with familial Parkinson's disease, progressive supranuclear palsy, and frontotemporal dementia.
Daida K et al.
Neurobiology of Aging, 2019
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study.
Tan MMX et al.
Brain : a Journal of Neurology, 2019
31324919 (PubMed )
Supplement: awz191_supplementary_data.pdf
LRP10 variants in Parkinson's disease and dementia with Lewy bodies in the South-West of the Netherlands.
Vergouw LJM et al.
Parkinsonism & Related Disorders, 2019
LRP10 in autosomal-dominant Parkinson's disease.
Chen Y et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2019
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study.
Quadri M et al.
The Lancet. Neurology, 2018
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