Associated Papers
De novo missense variants in FBXO11 alter its protein expression and subcellular localization.
Gregor A et al.
Human Molecular Genetics, 2022
34505148 (PubMed )
Supplement: table_s3_050721_ddab265.xlsx › Sheet1
De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder.
Gregor A et al.
American Journal of Human Genetics, 2018
De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies.
Fritzen D et al.
Human Genetics, 2018
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