Associated Papers
Parkinson's disease - genetic cause.
Cherian A et al.
Current Opinion in Neurology, 2023
RIC3 variants are not associated with Parkinson's disease in large European, Latin American, or East Asian cohorts.
Brolin K et al.
Neurobiology of Aging, 2022
Current Status of Next-Generation Sequencing Approaches for Candidate Gene Discovery in Familial Parkinson´s Disease.
Pillay NS et al.
Frontiers in Genetics, 2022
Genotype-Phenotype Correlations in Monogenic Parkinson Disease: A Review on Clinical and Molecular Findings.
Guadagnolo D et al.
Frontiers in Neurology, 2021
New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.
Puschmann A
Current Neurology and Neuroscience Reports, 2017
Genetic analysis of the RIC3 gene in Han Chinese patients with Parkinson's disease.
He D et al.
Neuroscience Letters, 2017
RIC3 variants are not associated with Parkinson's disease in French-Canadians and French.
Ross JP et al.
Neurobiology of Aging, 2017
Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes.
Sudhaman S et al.
Journal of Medical Genetics, 2016
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