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Paper Details

De novo missense variants in FBXO11 alter its protein expression and subcellular localization.
Hum Mol Genet
4
2022
C, FBXO11, FBXO11 missense variants, FBXO11 protein, FBXO11 variants, HEK293, HeLa cells, N, NDD, NDDs, Zn, behavioral anomalies, cytoplasm, developmental delay, facial dysmorphism, haploinsufficiency, hypotonia, intellectual disability, missense variants, neurodevelopmental disorder

Datasets

Release 1.2