Associated Papers
Bridging pleiotropic mechanisms in leprosy type-1 reactions and neurodegenerative diseases.
Fava VM et al.
Scientific Reports, 2025
41430073 (PubMed )
Supplement: 41598_2025_30734_MOESM2_ESM.xlsx › Variants
The characteristics of FBXO7 and its role in human diseases.
Zhong Y et al.
Gene, 2023
Parkin is the most common causative gene in a cohort of mainland Chinese patients with sporadic early-onset Parkinson's disease.
Jiang Y et al.
Brain and Behavior, 2020
Genetic variants of PARK genes in Korean patients with early-onset Parkinson's disease.
Youn J et al.
Neurobiology of Aging, 2019
Genetic analysis of ATP13A2, PLA2G6 and FBXO7 in a cohort of Chinese patients with early-onset Parkinson's disease.
Shen T et al.
Scientific Reports, 2018
Linking F-box protein 7 and parkin to neuronal degeneration in Parkinson's disease (PD).
Zhou ZD et al.
Molecular Brain, 2016
FBXO7 Y52C polymorphism as a potential protective factor in Parkinson's disease.
Chen CM et al.
Plos One, 2014
FBXO7 gene mutations may be rare in Chinese early-onset Parkinsonism patients.
Luo LZ et al.
Neuroscience Letters, 2010
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