Associated Papers
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
Current Status of Next-Generation Sequencing Approaches for Candidate Gene Discovery in Familial Parkinson´s Disease.
Pillay NS et al.
Frontiers in Genetics, 2022
Analysis of the LRP10 gene in patients with Parkinson's disease and dementia with Lewy bodies from Southern Italy.
Gagliardi M et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2021
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 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
Select a paper to view details