Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMouse Nr2f1 haploinsufficiency unveils new pathological mechanisms of a human optic atrophy syndrome.AuthorsBertacchi, Michele; Gruart, Agnès; Kaimakis, Polynikis; Allet, Cécile; Serra, Linda; Giacobini, Paolo; Delgado‐García, José M; Bovolenta, Paola; Studer, MichèlePublicationEMBO Molecular Medicine, 2019, Vol 11, Issue 8, pN.PAGISSN1757-4676Publication typeArticleDOI10.15252/emmm.201910291