De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder

Overview of attention for article published in American Journal of Human Genetics, July 2018

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LATEST ADDITIONS: De Novo Variants in the F-Box Protein FBXO11 in 20 individuals with a variable neurodevelopmental disorder https://t.co/kdOyQbsiiv

18 Apr 2023

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RT @JamesFasham: C08 #ESHG2022 Anne Gregor Initial publication - FBXO11 variants cause NDD https://t.co/dKGP0DeZAN Now understood - misse…

12 Jun 2022

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C08 #ESHG2022 Anne Gregor Initial publication - FBXO11 variants cause NDD https://t.co/dKGP0DeZAN Now understood - missense variants act through haploinsufficiency impairing SCF E3-Ubiquitin ligase complex & neuronal differentiation (due to NANOG ubi

12 Jun 2022

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De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder. https://t.co/tUNNzkfIQA

14 May 2019

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