Associated Papers
Real-world evaluation of gnomAD variant co-occurrence information for haplotype phasing in autosomal recessive disorders.
Kim J et al.
Human Genomics, 2025
41331868 (PubMed )
Supplement: 40246_2025_855_MOESM1_ESM.xlsx › Table_S1.
A Comprehensive Atlas of E3 Ubiquitin Ligase Mutations in Neurological Disorders.
George AJ et al.
Frontiers in Genetics, 2018
29491882 (PubMed )
Supplement: Table1.xlsx › Sheet1
A new F-box protein 7 gene mutation causing typical Parkinson's disease.
Lohmann E et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2015
FBXO7 Y52C polymorphism as a potential protective factor in Parkinson's disease.
Chen CM et al.
Plos One, 2014
Mutational analysis of FBXO7 gene in Parkinson's disease in a Taiwanese population.
Lin CH et al.
Neurobiology of Aging, 2013
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