Associated Papers
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss.
Khan H et al.
Scientific Reports, 2024
39271758 (PubMed )
Supplement: 41598_2024_71407_MOESM1_ESM.xlsx › HLMS03_het
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
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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