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

Paul, Maimuna S; Duncan, Anna R; Genetti, Casie A; Pan, Hongling; Jackson, Adam; et al.  American journal of human genetics Vol. 110, Iss. 1,  (Jan 5, 2023): 120-145.

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