{"identifier":"nobleid:/w1/20260526/9DA2FDA0","arkIdentifier":"ark:/48914/w1/20260526/9DA2FDA0","version":1,"workTitle":"Biallelic SZT2 mutations cause infantile encephalopathy with epilepsy and dysmorphic corpus callosum.","workType":"Journal Article","authors":"Basel-Vanagaite L, Hershkovitz T, Heyman E, Raspall-Chaure M, Kakar N, Smirin-Yosef P, Vila-Pueyo M, Kornreich L, Thiele H, Bode H","description":null,"workUrl":null,"existingDoi":"10.1016/j.ajhg.2013.07.005","createdAt":"2026-05-26T03:34:12.110879Z","canonicalUrl":"https://nobleid.org/ark:/48914/w1/20260526/9DA2FDA0.v1"}