by Institute of Molecular Biotechnology (IMBA) Graphical abstract. Credit: EMBO Molecular Medicine (2022). DOI: 10.15252/emmm.202215829 A multidisciplinary study led by Vanja Nagy (LBI-RUD/CeMM/Medical University of Vienna) and Josef Penninger (UBC/IMBA) characterized a novel gene, known as FIBCD1, to be likely causative of a new and rare neurodevelopmental disorder. Using data from two young patients with neurological symptoms,...
