Associated Papers
FBXO7 Pathogenic Variants in Early-Onset Parkinsonism: Insights from a Neuroimaging Perspective and Review of the Literature.
Şahin E et al.
Movement Disorders Clinical Practice, 2025
The characteristics of FBXO7 and its role in human diseases.
Zhong Y et al.
Gene, 2023
Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias.
Martínez-Rubio D et al.
International Journal of Molecular Sciences, 2022
Nearly Abolished Dopamine Transporter Uptake in a Patient With a Novel FBXO7 Mutation.
Kim EY et al.
Journal of Movement Disorders, 2022
35880381 (PubMed )
Supplement: jmd-22006-suppl.pdf
Neurodegeneration with Brain Iron Accumulation and a Brief Report of the Disease in Iran.
Hajati R et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques, 2022
Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect.
Correa-Vela M et al.
Annals of Clinical and Translational Neurology, 2020
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