Clinical and demographic characteristics of PINK1 mutation carriers-A meta-analysis
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference7 articles.
1. A heterozygous effect for PINK1 mutations in Parkinson's disease?;Abou-Sleiman;Ann Neurol,2006
2. Hereditary early-onset Parkinson's disease caused by mutations in PINK1;Valente;Science,2004
3. Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease;Rogaeva;Arch Neurol,2004
4. Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes;Bonifati;Neurology,2005
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1. Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1/PRKN-linked Parkinson’s disease;Brain;2022-12-07
2. Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1- and PRKN-linked Parkinson’s disease;2022-05-19
3. Basal Synaptic Transmission and Long-Term Plasticity at CA3-CA1 Synapses Are Unaffected in Young Adult PINK1-Deficient Rats;Frontiers in Neuroscience;2021-08-13
4. Novel ATP13A2 and PINK1 variants identified in Chinese patients with Parkinson’s disease by whole-exome sequencing;Neuroscience Letters;2020-08
5. ‘Atypical’ Parkinson's disease – genetic;International Review of Neurobiology;2019
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