Erratum: Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course (Brain (2019) 142 (3876–3891) DOI: 10.1093/brain/awz326)

Alessandro Esposito, Antonio Falace, Matias Wagner, Moran Gal, Davide Mei, Valerio Conti, Tiziana Pisano, Davide Aprile, Maria Sabina Cerullo, Antonio De Fusco, Silvia Giovedì, Annette Seibt, Daniella Magen, Tilman Polster, Ayelet Eran, Sarah L. Stenton, Chiara Fiorillo, Sarit Ravid, Ertan Mayatepek, Hava Hafner, Saskia Wortmann, Erez Y. Levanon, Carla Marini, Hanna Mandel, Fabio Benfenati, Felix Distelmaier, Anna Fassio and Renzo Guerrini. Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course. Brain 2019; 142: 3876–3891. doi:10.1093/brain/awz326. The authors apologize for an error in the protein translation description of the c.7518-1G4A splice variant in the ‘Effect of DMXL2 mutations on mRNA and protein expression’ section. The sentence should read: Finally, the splice variant c.7518-1G4A, identified in homozygosity in Patient 3-II:5, resulted in the skipping of exon 31, leading to a frameshift and premature termination of protein translation (p.Trp2507Argfs\4; Supplementary Fig. 4C).