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, March 2023

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RT @DiseaseGenes: Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotoni…

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy https://t.co/3Gt8fT9bXH

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