Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder. - Komatsu K; Sugie A; Nitta Y; Osaka J; Mansoor Hussain UH; Kubota M; Shimozawa N; Carter MT; J G Zwijnenburg P; Waisfisz Q; Boschann F; Horn D; et al. (European journal of human genetics : EJHG, 2026)