Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease
Author:
Funder
National Natural Science Foundation of China
Publisher
Elsevier BV
Subject
Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience
Reference37 articles.
1. Use of antidepressants and the risk of Parkinson’s disease: a prospective study;Alonso;J Neurol Neurosurg Psychiatry,2009
2. NUS1 mutation in a family with epilepsy, cerebellar ataxia, and tremor;Araki;Epilepsy Res.,2020
3. The genetic architecture of Parkinson's disease;Blauwendraat;Lancet Neurol,2020
4. Replication assessment of NUS1 variants in Parkinson's disease;Bustos;Neurobiol. Aging,2021
5. Genetic analysis of NUS1 in Chinese patients with Parkinson's disease;Chen;Neurobiol. Aging,2020
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Novel NUS1 variant in a Chinese patient with progressive myoclonus epilepsy: a case report and systematic review;Neurological Sciences;2023-05-30
2. The association between LIN28A gene rare variants and Parkinson’s disease in Chinese population;Gene;2022-06
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