Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy

Overview of attention for article published in American Journal of Human Genetics, December 2022

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news: 10 news outlets
blogs: 1 blog

twitter: 28 X users
reddit: 3 Redditors

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mendeley: 41 Mendeley

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RT @interactivefly: Paul, M. S., Duncan, A. R., Genetti, C., ..., Chao, H. and Agrawal, P. B. (2023). Rare EIF4A2 variants are associated…

Paul, M. S., Duncan, A. R., Genetti, C., ..., Chao, H. and Agrawal, P. B. (2023). Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy. Am J Hum Genet 110(1): 120-145…

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy https://t.co/LdUUhKZFXL

RT @DiseaseGenes: RT @platzer_k: #EIF4A2 is a new AD & AR #MorbidGene for a NDD. Both LoF & GoF identified as underlying mechanisms. @Maimu…

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