Associated Papers
The characteristics of FBXO7 and its role in human diseases.
Zhong Y et al.
Gene, 2023
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
Novel compound heterozygous FBXO7 mutations in a family with early onset Parkinson's disease.
Lorenzo-Betancor O et al.
Parkinsonism & Related Disorders, 2020
Select a paper to view details