Two rare mutations in homozygosity synergize to silence TREX1 in Aicardi-Goutières syndrome. - Rubin T; Bernier S; Hoon Lim LS; Salman MS; Leung E; Mhanni A; Marles S; Greenberg C; Perez A; Sun Y; Angers I; Vinh DC; et al. (Frontiers in immunology, 2025)